The Tishchenko reaction mediated by organo-f-complexes: the myths and obstacles

For over a century, the Tishchenko reaction has been a valuable technique for synthesizing esters from aldehydes, serving a variety of applications in different domains. Beyond the remarkable advances in organoactinide and organolanthanide chemistry over the past two decades, there has been a significant increase in the research of the electrophilic d0/fn chemistry of organoactinide and organolanthanide compounds due to the captivating interplay between their structure and reactivity, and their exceptional performance in various homogeneous catalytic processes. The remarkable influence of ligand design, both in terms of steric hindrance and electronic properties, on the catalytic activity of organo-f-element complexes in organic transformations is well-established. However, the traditional view was that the significant oxophilicity of actinide and lanthanide complexes makes them unfavorable for reactions involving oxygen because of catalytic poisoning and their applications have been relatively limited, primarily focused on hydroalkoxylation, small-molecule activation, and cyclic ester polymerization. This review dissects the intricate interplay between ligand design and catalytic activity in actinide and lanthanide complexes, specifically in the context of the Tishchenko esterification.


Introduction
Esters are versatile chemical compounds with applications in a variety of industries like plastics, solvents, fragrances, avors, and even pharmaceuticals and agriculture.Traditionally, esters were synthesized by reacting carboxylic acids and alcohols with catalysts like acids 1 or metals, 2 generating the desired ester and water.However, this process oen necessitates specic techniques or excess starting materials to overcome the low product yield owing to the equilibrium favoring both the ester and byproducts. 3,4Unfortunately, using these traditional methods results in signicant waste and underutilizes the starting materials, raising concerns about both impacts on the environment and efficiency.Back in 1887, a pioneering chemist named Rainer Ludwig Claisen discovered a remarkable reaction: the Claisen condensation. 5,6This ingenious process forges carbon-carbon bonds, bridging esters or other carbonyl compounds together.Ever since its discovery, the Claisen condensation has captivated chemists worldwide, inspiring countless investigations and innovations (Scheme 1).
Claisen pioneered the pathway for aldehyde esterication by revealing their dimerization potential in the presence of sodium alkoxides.Building on this basis, Tishchenko established the process as an overall strategy, using various metal alkoxides (Al or Mg) to catalyze the reaction across an additional range of aldehydes. 3The Tishchenko reaction, as demonstrated by routes A and B in Scheme 2, is versatile in terms of starting materials.Route A uses two similar aldehydes to form a symmetrical ester (1), while route B allows the combination of different aldehydes to yield a mixture of products (1-4). 3,4he widely accepted mechanism of the Claisen-Tishchenko reaction begins with the aldehyde coordination to the Lewis acidic aluminium alkoxide catalyst (as shown in Scheme 3).The coordinated hemiacetal (A) is formed by shiing an alkoxide group to the aldehyde.Another aldehyde molecule then bonds to the central aluminium atom.The hydride transfer occurs from the hemiacetal to the new aldehyde, releasing a mixed ester, and the reduced aldehyde now acts as a new alkoxide ligand for the aluminium.This process is repeated as a third aldehyde molecule interacts with the new aluminium complex (B), transferring the previously created alkoxide group to the aldehyde.Aer the cycle is completed, symmetrical ester (1) is cleaved, allowing the catalyst to start another cycle (Scheme 3).
Mechanistically, the Tishchenko reaction is part of a family of reactions involving alkoxide-driven transformations of aldehydes, including Cannizzaro, 7,8 Meerwein-Ponndorf-Verley, 9 and Oppenauer oxidation. 10A diverse range of catalysts, both homogeneous and heterogeneous can be utilized to promote the Tishchenko reaction.The Tishchenko reaction has been catalyzed by many metal complexes 3,4,6,11 and solid-phase catalysts. 12The bidentate aluminum complexes like sodium organoaluminate complex, 13 aluminum alkoxide complexes, 14 and N,O-bidentate aluminum complexes 15 a very potent catalyst considerably aided the Tishchenko reaction.Other catalysts employed include alkali and alkaline earth metal oxides (including Grignard-type compounds), 16,17 lanthanoids, 6,18 and transition metals. 19,20The development of heterogeneous In 2018, he joined as an assistant professor in the department of applied chemistry in Govt.Engineering College, Jabalpur.Currently, he is an assistant professor at the Vellore Institute of Technology (VIT), Vellore.His current research interests are centered on the synthesis and reactivity investigation of early transition metal complexes with the goal of nding novel applications in widely applicable organic transformations and small molecules (CO 2 , H 2 O etc.) activation.
catalysts for the Tishchenko reaction has mostly focused on alkaline earth metal oxides and different types of alumina.However, these catalysts tend to be very slow or only show reactivity in extremely stringent reaction conditions.
By the mid-twentieth century, interest in the Tishchenko reaction had grown because of the emergence of different variations of the Tishchenko reaction, and substantial growth in this topic in recent years.A well-known process called the aldol reaction bridges two molecules that contain carbonyl to form a new C-C bond. 21,22A b-hydroxy ketone was formed, regardless of whether the two are aldehydes or a combination of aldehydes and ketones in the aldol reaction.The Tishchenko reaction has led to two famous modications, each adding a distinctive twist to its core principle: the aldol Tishchenko reaction, 23,24 which incorporates it with the classical C-C bond formation of the aldol reaction, and the Evans-Tishchenko reaction 25,26 which was known for its diastereoselective reduction of b-hydroxy ketones.The aldol Tishchenko reaction was a two-step reaction where the rst step comprised an aldol reaction employing two different aldehydes, and the second step comprised the subsequent coordination of another aldehyde, which was then followed by a Tishchenko-type hydride transfer (Scheme 4).In Evans-Tishchenko reaction catalytic samarium iodide was employed to yield 1,3-antidiol monoesters 3,27-29 (Scheme 5).This reaction can take place with enolizable aldehydes (aldehyde trimerization), or it can take place with ketones (formation of 1,3-diol monoesters).1][32][33][34][35][36][37][38][39][40][41][42] Other options for ester synthesis such as Favorskii, 43 Fischer, 44,45 Steglich, 46 and Yamaguchi 47 reactions were available, but their limitations made them unsuitable for an industrial-applications.From an atom economy perspective, Tishchenko reaction-based ester synthesis outperforms typical methods, which oen yield undesirable leaving groups and side products that do not contribute to a nal product.The Tishchenko reaction has the enticing technical advantage of being able to be carried out by aldehyde as a reactant and the solvent and pushed almost to completion, without the need for any additional purication processes.Modifying the parameters that govern the reaction conditions (temperature, pressure, solvent, and catalyst) can exert a signicant inuence on the product distribution of the Tishchenko reaction.The emphasis on the coordinating metal and its surrounding ligands led to the development of diverse catalysts for the Tishchenko reaction.While transition metal catalysts such as [Cp 2 ZrH 2 ] (5), 48 [H 2 Ru(PPh 3 ) 2 ] (6), 49 and K 2 [Fe(CO) 4 ] (7) 50 exhibited efficacy in Tishchenko reactions, they were not without their limitations.
Inner transition organometallic compounds have emerged as promising alternatives to traditional transition metal complexes, owing to a need for novel catalysts and the unique properties of actinides and lanthanides.Recent research has focused signicant emphasis on the development of organoactinide and organolanthanide complexes as catalysts for Tishchenko reactions.This increased interest stems from their advantageous properties, including high Lewis acidity, high coordination numbers, relatively polar metal-ligand bonding, a tunable coordination sphere around the metal center, a plethora of coordination geometries, and environmental friendliness.2][53] The distinctive reactivities of organoactinide and organolanthanide compounds oen complement those observed in the main group and, transition metal.An example of this is the fact that, unlike the anti-Markovnikov addition products generated by transition metal precatalysts, actinide complexes showed Markovnikov selectivity when hydrothiolating terminal alkynes. 54,55The prevalence of unique oxidation states (+3 in lanthanides and +4 in early actinide (Th)) precludes the conventional catalytic routes of oxidative addition and reductive elimination commonly observed in transitionmetal complexes.][58][59][60] The strong affinity of actinide and lanthanide centers for oxygen-containing substrates posed a signicant challenge in organo-f-chemistry.The formation of stable and unreactive oxygen-metal bonds hinders the transformation of these substrates, contributing to the historical lag observed in this eld compared to d-block metal complexes.7][68] This delay can also be attributed to the limited research efforts dedicated to this eld.

Actinide complexes catalysed Tishchenko reactions
Over the last two decades, both anionic and neutral organoactinide complexes have been the subject of intense research for their potential to function as catalysts in a variety of organic reactions.Some of these reactions were polymerization of alkenes, 93,112 oligomerization, 113,114 intermolecular hydroamination, 69,77,78,115 hydrosilylation of terminal alkynes, 73,116 and hydrophosphination, 69 etc.However, because of the strong oxophilicity of the actinide complexes (208.0 kcal mol −1 for ThO and 181.0 kcal mol −1 for UO), all substrates containing oxygen atoms, especially aldehydes, were eliminated and the predicted poor activity of these complexes was attributed to the foreseeable oxygen-actinide interaction.
Andrea et al. described that organoactinide-mediated catalytic Tishchenko reactions involving two identical or different aldehydes resulted in the formation of symmetric (1 and 2) or asymmetric (3 and 4) esters, respectively (Scheme 6).In order to provide a suitable mechanism for the Tischenko reaction and to imply the process's application, two organoactinide complexes, Cp* 2 ThMe 2 (8) and Th(NEtMe) 4 (9), were investigated.By substituting an alkoxo ligand (OR) for one of the methyl groups in Cp* 2 ThMe 2 , the hydrogenolysis efficiency was reduced by a factor of 4000.Intriguingly, substrate activity was determined by the closeness of phenyl group substituents to a metal center.The reduced activity of the substrate with ortho substituent relative to para isomers may be ascribed to steric hindrance.The two organoactinide complexes (8 and 9) were discovered as highly to moderately active (yields 85-65%) in the catalytic dimerization of benzaldehyde and other substituted benzaldehyde to give the corresponding ester with no by-products.In the Tishchenko reaction, tweaking the ratio of reactants allowed to ne-tune the proportions of the four possible products.An intriguing result of the reaction between two different aldehydes was the appearance of four possible isomers.As an illustration, when p-tolualdehyde and benzaldehyde reacted, as expected, the less reactive p-tolualdehyde participated in the catalytic process to a lesser extent catalytic process, resulting in benzoyl benzoate consistently being the main product.A kinetic and thermodynamic investigation of complex 8 was carried out to propose a plausible mechanism for the reaction and learn about the effects of aldehyde, catalyst, and temperature on the reaction rate.
As seen in eqn (1), the reaction had a rst-order dependence on both catalyst and aldehyde.According to thermodynamic studies, the energy of activation (E a ), enthalpy of activation (DH ‡ ), and entropy of activation (DS ‡ ) for the rate-determining step revealed 7.16 ± 0.40 kcal mol −1 , 6.5 ± 0.4 kcal mol −1 , and −48.8 ± 0.4 eu, respectively.At the rate-determining step, the high negative entropy value indicated a highly ordered transition state.A primary isotopic effect was observed with k H / k D = 2.7, indicating that hydride transfer was involved in the rate-determining step.
A plausible mechanism for the Tishchenko reaction was presented in Scheme 7 based on the kinetic and thermodynamic data. 94The catalytic cycle commenced with the formation of the metal alkoxy intermediate (A 1 ) via a four-center transition state initiated by a thermodynamically favorable interaction between two aldehyde molecules and precatalyst 8. 94,117,118 The complex (A 2 ) was formed by the second insertion of an aldehyde into the thorium-alkoxide bond.In a subsequent step, the ester (A 4 ) was produced by the metathesis of complex (A 2 ) with an additional aldehyde through a six-membered transition state (A 3 ).The catalytic insertion of an aldehyde into a thorium alkoxo bond was followed by a hydride transfer reaction with another aldehyde via a plausible six-centered transition state, Scheme 6 Synthesis of Cp*ThMe 2 (8) and Th(NEtMe) 4 (9).
which produced ester (1) and regenerated the active complex (A 5 ) (Scheme 7).An actinide-alkoxy bond, long considered to constitute an impasse in the use of actinide complexes as catalysts, was activated during the process.Hence this was the rst example of actinide complex-mediated catalytic coupling of aldehyde.The organoactinide complexes 8, 9, and 10 were efficient precatalysts for the chemoselective dimerization of aldehydes, leading to the formation of the esters in moderate to high yields.The corresponding esters formed via the reaction of these complexes with an excess of aldehyde in toluene or benzene (aldehyde : catalyst = 100 : 1) at room temperature.Sharma et al. proposed a strategy in which a metal-oxygen bond was thermodynamically inserted with a substrate to generate a second metal-oxygen bond with equal bond energies, while entropy being the major parameter controlling the reaction. 98In the presence of Argon, Me 2 SiCp 00 2 ThCl 2 -2LiCl-2DME was slowly added to n-butyl lithium at −30 °C.The reaction was warmed to 0 °C and stirred for an additional 30 minutes.The condensed pentane was removed with a vacuum, and the orange-brown solids were dried in a vacuum for 13 hours.The solid was collected by cold ltration, and re-crystallization from DME formed a pale yellow solid.[121] Enhanced reaction rates were reported when the same dimerization process was conducted at a marginally elevated temperature of 35 °C.According to the results, the rate of dimerization rises as the coordinative unsaturation of the organoactinide complexes utilized in this research increases, with 10 being the highest, followed by 9 and 8, respectively.Kinetic measurements were conducted to enhance comprehension of the impact of auxiliary ligands, as well as the inuence of the aldehyde and catalyst on the rate of the reaction.The dimerization of aldehydes promoted by complexes 8 and 10 can be expressed as eqn (2).
Since complex 10 readily binds to other molecules (highly coordinatively unsaturated), a limiting substrate : catalyst ratio was present to achieve the fastest reaction for which the optimal substrate : catalyst ratio was around 300 to 1.For complexes 8 and 10, at constant concentrations of benzaldehyde and catalyst, similar kinetic dependence was observed on aldehyde and the catalyst over the range of temperature studied (35-95 °C).The activation parameters determined by Arrhenius and Eyring analysis were E a = 7.16 kcal mol −1 , DH ‡ = 6.58, kcal mol −1 , DS ‡ = −48.8eu and E a = 3.47 kcal mol −1 , DH ‡ = 2.80 kcal mol −1 , DS ‡ = −65.2eu for complexes 8 and 10 respectively. 98Complex 10 had a higher negative DS ‡ , indicating a more structured transition state, which facilitated a higher degree of coordinative unsaturation.To evaluate the effect of substituents on the benzene ring while the dimerization reaction was taking place, the thermodynamic parameters (E a , DH ‡ , and DS ‡ ) of the rate-determining step (RDS) were measured and calculated for the meta-and para-substituted benzaldehyde with the electronwithdrawing chlorine and the electron-donating methyl group using complex 10 (Table 1).From Table 1, it can be concluded that the presence of the electron-withdrawing group on the aromatic ring resulted in a slightly lowered E a compared to the presence of the electron-donating group on the aromatic ring.For complex 10, a primary isotopic effect was observed using deuterated benzaldehyde with K H /K D = 2.7, revealing that hydride transfer was involved in the RDS. 122When complexes 8, 9, and 10 were used, stoichiometric reactions between actinide complexes and benzaldehyde yielded the stoichiometric amounts of esters.Complexes 8, 9, and 10 displayed remarkable catalytic activity in the selective dimerization of aldehydes, resulting in desired esters with excellent chemoselectivity and no by-products.The observed catalytic activity trend was 10 > 9 > 8, maybe due to the differences in coordinative unsaturation around the metal center (Table 2).
Scheme 9 depicts a plausible mechanism for the selective dimerization of aldehydes facilitated by the organothorium complex 10. 98 The catalytic process was initiated by adding two   equivalents of aldehyde through a thermodynamically favorable four-centered transition state (DH calc = −68 kcal mol −1 ), resulting in the corresponding bis(alkoxo) complex (B 1 ).Complex (B 2 ) was formed when additional aldehyde molecules were added to the thorium-alkoxide bond.Complex (B 2 ) did not add any additional aldehyde molecules, but rather eliminated the rst ester (B 4 ) in stoichiometric amounts, either by hydride transfer to an incoming aldehyde through a six-centered transition state (B 3 ), with the production of the active catalytic complex (B 5 ), or by b-H elimination and rapid insertion of an aldehyde to produce the active complex (B 5 ).The catalytic cycle started with the insertion of an aldehyde molecule to the thorium-alkoxide bond of complex (B 5 ) via a four-centered transition state (B 6 ), similar to that of complex 10, to produce complex (B 7 ), which further performed a hydride transfer to another aldehyde via a six-centered transition state (B 8 ) as the RDS, thereby regenerating the active catalyst and symmetrical ester as a product (1).A b-hydrogen elimination reaction from (B 7 ) could generate the symmetrical ester product (1) as well as a Th-H complex (B 10 ), which may react with an aldehyde to generate the active catalytic species (B 5 ).The b-hydrogen elimination reaction was found to have a higher enthalpy than the reaction involving a six-centered transition state (+56 and −47 kcal mol −1 , respectively), which showed that the bhydrogen elimination pathway was not the primary termination pathway (Scheme 10).
Scheme 10 depicts the two potential reaction pathways available to the aldehyde upon interaction with complex (B 7 ).In the rst pathway (a), an additional insertion led to the formation of the complex (B 11 ), while in the second pathway (b), a hydride transfer produced complex (B 5 ) and the ester product (1).The entropy of activation indicated that hydride transfer was more preferred than the additional aldehyde insertion.The Eyring plots and complex 10 were used to ascertain that the DS ‡ of activation for all the aldehydes being studied was −65 eu.
This result revealed a highly organized transition state with substantial bond-making to compensate for bond-breaking.As the process approaches the transition state, it undergoes a high degree of entropic reorganization.Despite attempts to synthesize complex (B 11 ) using independent stoichiometric processes with a bisalkoxo complex and an aldehyde, the desired complex (B 11 ) remained elusive.This was surprising from a chemical kinetics standpoint, implying that the aldehyde may be hindered from reaching the metal center due to steric hindrance.In pathway (a), when a four-centered transition state formed, the benzylic carbon should shi to a spatial position close to the oxygen atom bonded to the metal, producing a conned transition state, whereas, in pathway (b), the benzylic carbon should shi to a position proximal to the benzylic hydrogen, resulting in a less hindrance between the incoming aldehyde and the alkoxo group.Comparing the calculated activation energy for pathway a (8.5 kcal mol −1 ) to the measured value for pathway b (3.47 kcal mol −1 ), supported that complex (B 5 ) and the dimer were formed during the reaction.The lower values of E a , and DH ‡ , as well as the reduced negative value of DS ‡ were obtained for complex 10 as compared to complex 8, demonstrating the benecial effect of incorporation of the bridging ligand resulted in a complex with higher coordinative unsaturation.The use of a constrained-geometry catalyst (CGC) with bridged cyclopentadienyl ligands enhanced the catalytic activity of the corresponding actinide complexes by opening the coordination sphere.The results of this study have opened up a novel pathway for research into the catalytic activity of organoactinide complexes using oxygenated substrates.
Complex 8 promoted "cross-Tishchenko" reaction in which two distinct aldehydes (benzaldehyde and p-tolualdehyde) reacted to form four possible esters (Scheme 2).The ndings (Table 3) were consistent with the expected inuence of aldehyde reactivity on product selectivity.Since benzaldehyde was more active, it predominantly forms a symmetrical ester (1).
In order to increase the catalyst activity of actinide complexes in the Tishchenko reaction, Karmel and coworkers introduced imidazoline-2-imine (Im R N) based actinide catalysts. 99,100The imidazolin-2-iminato ligands were potent 2s,4pelectron donor ligand.[125][126][127] 3. N-Heterocyclic iminato actinide complexes and neutral lanthanide complexes catalyzed Tishchenko reaction  (8) with the immediate evolution of CH 4 gas (Scheme 11). 100 The X-ray structure analysis conrmed the central thorium was surrounded by one methyl, one imidazolin-2-iminato moiety, and two Cp* ligands in both complexes 13 and 14, completing the tetrahedral geometry.Complexes 13 and 14 displayed short Th-C methyl bond lengths compared to complex 8.The Th-N imine bond lengths of complexes 13 and 14 were shorter than the Th-N amido bond in Cp* 2 Th(NHR)(Cl) complexes (Scheme 11).
In the catalytic Tishchenko reaction, Menashe et al. discovered that enhancing the electron density of a metal complex improved its activity towards aldehydes. 128The Tishchenko reaction was performed with various aldehydes including aromatic, heteroaromatic, cyclic, and aliphatic aldehydes.Complex 13 exhibited a slightly greater level of activity compared to complex 14.This can be attributed to the strong electron-donating nature of the imidazolin-2-iminato ligand.It was important to measure the equivalents of precatalyst involved during one catalytic cycle, and the number of active sites present per unit of catalyst for a better understanding of the reaction mechanism.The poisoning experiments carried out using isopropanol suggested that the catalytic activity was reduced to 25% while the catalyst 13 to isopropanol ratio was maintained at 1 : 0.25.However, keeping the catalyst-toisopropanol ratio to 1 : 0.50, the activity decreased to 50% from the actual value.Similar poisoning experiments with catalyst 8 were found to decrease the activity by 12.5%, keeping the catalyst to isopropanol ratio of 1 : 0.25.When the catalyst 8 to isopropanol ratio was maintained at 1 : 0.50, it led to decreased activity of 1/4 th of the initially determined value without isopropanol.So, it was concluded that catalyst 8, containing -CH 3 groups, was active in the catalytic process.Generally, higher catalytic activity was observed in aldehyde with electron-withdrawing groups which led to higher conversion in a short period of time.For example, benzaldehyde was substituted with p-NO 2 , m-NO 2 , p-CN, and p-CF 3 , leading to a higher yield.The presence of the electron-donating groups like methyl or methoxy on the aldehyde made the reaction less efficient, resulting in a lower yield of the desired product.The aromatic and heteroaromatic aldehydes needed a higher reaction time for completion (Table 5).Experimental investigations utilizing precise stoichiometric concentrations of precatalyst 13 and aldehydes provided evidence supporting the coordination insertion mechanism outlined in Scheme 12. 100 In the rst step of the catalytic cycle, the incoming aldehyde was inserted into the Th-C bond, resulting in the thorium alkoxo intermediate (C 1 ).Aer the insertion of a second aldehyde monomer into the Th-O bond, the intermediate (C 2 ) was formed.This intermediate, upon hydride transfer with another aldehyde via the sixmembered transition state (C 3 ), led to the catalytically active thorium alkoxo complex (C 4 ) as well as 1 equivalent of the methylated ester.Insertion of the incoming aldehyde into the Th-O bond of (C 4 ) resulted in the formation of the intermediate (C 5 ), which then reacts with another one equivalent of aldehyde via a hydride transfer in a six-membered transition state (C 6 ) to give the respective ester (1) during regeneration of the catalytically active thorium alkoxo species (C 4 ).
This investigation additionally examined the reactivity of thorium(IV) complex 13 in the context of the crossed Tishchenko reaction.When equimolar amounts of two aromatic aldehydes were used in the crossed Tishchenko reaction, the resulting ester mixture showed an almost uniform distribution of all four potential products, indicating a competitive dynamic between the aldehydes (1-4) (Scheme 2).The addition of an excess of different aldehyde (R 0 CHO) raised the product distribution to the symmetrical ester R 0 CH 2 OCOR 0 (2) (Scheme 2).However, selectivity for the remaining two asymmetrically substituted esters (3-4) remained rather constant, indicating a non-   6), and 1.319(9) Å, for 17-22 respectively (Fig. 1).In early studies, Andrea et al. showed the reactivity of Cp* 2 ThMe 2 towards aromatic aldehydes, which exhibited strong catalytic activity and tolerance for several functional groups. 95 addressing the fundamental question of whether post-metallocene actinide catalysts exhibit reactivity not only towards aromatic aldehydes but also towards cyclic and branched aliphatic aldehydes.To nd a catalyst with the highest catalytic applicability towards the Tishchenko reaction, catalytic studies were performed with benzaldehyde as the model substrate.Thorium complexes were found superior compared to respective uranium analogs.The thorium(IV) complex [(Im Dipp N)Th {N(SiMe 3 ) 2 } 3 ] (19) demonstrated the highest catalytic turnover in the series towards a variety of substrates including aromatic, cyclic, acyclic, polyaromatic, and branched aliphatic aldehydes.The poisoning tests were carried out to assess the percentage of precatalyst that was active in the reaction.Poisoning studies with isopropanol demonstrated that catalyst 19 was actively involved in the catalytic process.Experiments using catalytic amounts of [(Im Dipp N)Th{N(SiMe 3 ) 2 }] (19) and benzaldehyde showed that two aldehyde units could bind to the Th-N(SiMe 3 ) 2 , resulting in twice the amount of N(SiMe 3 ) 2 a-substituted ester (D 4 ).This product was then characterized using a mixture of 1 H NMR, 13 C NMR, 29 Si NMR, and mass spectroscopy analysis.The space-lling models were used to explore the steric hindrance surrounding the corresponding actinide core, which played a crucial role in catalytic activity.The cavities that were formed by the carbon atoms of the R-substituents of both the imidazolin-2-iminato ligand and the carbon atoms of the bis(trimethylsilyl)amido ligands varied from 3.6 to 4.5 for complexes 17, 18, and 20-22; however, the complex [(Im Dipp N) Th{N(SiMe 3 ) 2 } 3 ] (19) has a larger cavity (5.7), which corresponds to the higher activity.The catalytic cycle started with the coordination of two units of aldehydes to Th-alkoxo species (D 1 ) to afford the intermediate species (D 2 ). 99The intermediate (D 2 ) underwent a reaction with another aldehyde, resulting in the formation of the Th-Oxo compound (D 5 ) via a six-member transition state (D 3 ).This process involved the elimination of one equivalent of an ester molecule (D 4 ).The desired ester (1) was successfully synthesized by incorporating an aldehyde component into the intermediate (D 6 ) through a six-membered transition state (D 7 ) and regenerating the catalytically active Th-Oxo species (D 5 ).The hydride transfer step was identied as the slowest step in the reaction pathway (Scheme 14).
When complex 19 was employed as a catalyst in the crossed Tishchenko reaction with a 1 : 1 ratio of aromatic/polyaromatic and cyclic/branched aliphatic aldehydes, the resulting products were symmetrical and asymmetrical esters in almost equal quantities (1-4).Surprisingly, employing a 1 : 1 ratio of RCHO and R 0 CHO, the reaction favored the asymmetric ester (RCH 2 -OCOR 0 ) (3) aer 2 hours, leaving only a trace of the other symmetric ester (R 0 CH 2 OCOR 0 ) (2).However, over time (24 hours), the symmetric esters (RCH 2 OCOR (1) and R 0 CH 2 OCOR 0 ) (2) gain precedence, with traces of another asymmetric ester (R 0 CH 2 OCOR) (4).The nal product distribution was approximately 25% RCH 2 OCOR 0 (3), 5% R 0 CH 2 OCOR (4), 33% RCH 2 -OCOR (1), and 35% R 0 CH 2 OCOR 0 (2).This implied that the crucial intermediate (D 5 ) (Scheme 14), preferentially interacts with an aliphatic aldehyde.This product can then react with another aromatic aldehyde to complete the catalytic cycle, which is indicated by the initial asymmetric ester formation.As the reaction advanced, increasing amounts of a symmetrical ester revealed competition between the two aldehydes present.To favor the synthesis of the desired, symmetrical ester, the higher proportion of the aromatic aldehyde (RCHO : R 0 CHO = 20 : 1) was utilized to avoid the formation of an asymmetrical ester.Aliphatic aldehydes, with their superior hydride-donating ability, outcompete electron-withdrawing aromatic aldehydes (better hydride acceptors) for interaction with the catalyst.This control over the reaction pathway leads to the selective formation of the symmetric ester.This suggested that the ratedetermining step (RDS) in the catalytic cycle was hydrogen transfer.When the amount of aliphatic aldehyde (R 0 CHO) decreases (over 95% of the target product formed), the excess aromatic aldehyde (RCHO), acts as a slower hydride acceptor, which gradually forms the symmetrical ester, reaching complete conversion aer 24 hours (Table 4). 992.Benzimidazolin-2-iminato actinide complex based tandem proton-transfer esterication (TPTE) Liu and co-workers have developed a unique series of ligand systems through alterations to the imidazolin-2-imine backbone, intending to impact the catalytic effectiveness of actinide complexes.53,101 The synthesized ligands were used to form a new class of actinide complexes by treating with actinide metallacycles [(Me 3 Si) 2 N] 2 An-[k 2 (N,C)-CH 2 Si(CH 3 ) 2 N(SiMe 3 )] (An = Th (15) and U (16)) to generate a series of actinide complexes (Scheme 15).Solid-state studies of all complexes revealed identical isomorphous pseudo-tetrahedral geometries and bonding characteristics to the corresponding imidazolin-2-iminato actinide complexes (23-30).53,99 Tandem proton-transfer esterication (TPTE) represented a novel approach for the synthesis of asymmetric esters by coupling aldehydes and alcohols (Scheme 16).The benzimidazolin-2-iminato actinide(IV) complexes (23-30) were utilized for the Tishchenko reaction.The reaction conditions were optimized by carrying out the reactions between PhCHO/CH 3 OH/ 27.The threefold increase in the molar ratio of the PhCHO/ CH 3 OH from 1 : 1 to 3 : 1, enhanced the yields of methyl benzoate, indicating the advantageous presence of aldehyde in the reaction mixtures.While increasing the methanol amount in the mixture from 1/1 to 1/3, a reduced yield of the asymmetric ester demonstrated the negative inuence of alcohol present in the reaction mixture.In general, thorium complexes exhibited higher activity compared to uranium analogs.In the tandem proton transfer esterication reaction, a special ketone called a,a,a-tri-uoroacetophenone (TFMAP) used as sacricial ketone to avoid unwanted symmetrical products (Fig. 2 and Table 6).
Taking into consideration the ndings, a viable mechanism was suggested. 53,101The catalytic cycle commenced with the reaction of complex 27 and alcohol, leading to the formation of actinide alkoxide species (E 1 ) (Scheme 17).The catalytically active species (E 1 ) was inserted into the carbonyl group of incoming aldehydes to form an intermediate (E 2 ).The intermediate (E 2 ) coupled with another approaching aldehyde via a six-member transition state (E 3 ) to yield actinide alkoxide species (E 5 ) and the target asymmetric ester (E 4 ).Proton transfer  Review RSC Advances takes place between the (E 5 ) and excess alcohol, which regenerates the active catalyst (E 1 ).
Substrates having electron-withdrawing groups were more active than those having electron-donating substituents.The inclusion of potent electron-donating groups like 4-MeO-, 4-Me 2 N-signicantly reduced the reactivity of the active species.The steric nature of the substituents had a notable impact on the reaction.As the hindrance increased, the yield decreased because bulky aldehydes or alcohols were unable to easily get to the thorium center.The N-heterocyclic imine's central structure can be altered by varying the size of the ring.Through the incorporation of the perimidin-2-iminato (Pr R N − ) moiety, a remarkable achievement was made in expanding the ring and modifying the backbone on a single platform. 102

Perimidine scaffold and seven-membered Nheterocyclic iminato actinide complexes catalyzed Tishchenko reaction
The at structure of the ve and six-membered N-heterocyclic iminato auxiliary ligands imposes limitations on the spatial  arrangement of the wingtip.The incorporation of a sixmembered ring instead of a ve-membered heterocycle moiety, as detailed in the study by Ghatak et al., led to the development of the Perimidine scaffold.This modication resulted in a notable increase in the activity of organoactinide complexes. 102A novel N-heterocyclic iminato core architecture featuring a seven-membered ring was designed to address the rigidity challenges associated with planar heterocyclic frameworks.This innovative design incorporated a torsional twist mechanism to alleviate ring strain and enhance functionality.This study showed the simple synthesis of two Th(IV) complexes, one with a six-membered N-heterocyclic iminato framework and the other with a new seven-membered ring ligand.The impact of ring size on the catalytic activity of an organoactinide complex was investigated in this study.The actinide complexes 31 and 32 were synthesized in toluene using a one-pot reaction between complex 8 with the respective N-heterocyclic imine ligand, which resulted in the immediate evolution of methane (Scheme 18).The X-ray structure study of complex 31 revealed that the distance between the Th-N1 imine bond (2.225 Å) and other imidazolin-2-iminato thorium structures was comparable, showing that the Th-N bond has a high bond order (Fig. 3).The Th-Cp* centroid distances were 2.57 Å and 2.56 Å, respectively, while the Th-CH 3 = 2.488 Å, all of which were shorter than those observed for Cp* 2 Th(CH 3 ) 2 .The crystal structure of the free ligand L 2 H revealed the axial symmetry resulting from the twisting of the seven-membered N-heterocyclic imine rings (42.2°torsional angles between two phenyl rings).The distances between the Th-N bond and the Th-Cp*centroid for complex 32 were 2.21, 2.55, and 2.58 Å respectively (Fig. 3).The equivalent bond distances observed in complexes 31 and 32 indicated that these complexes possess comparable electrical properties.Complex 31 and 32 were employed as a precatalyst to efficiently transform aldehydes into their respective esters via the Tishchenko reaction, achieving excellent yields even at ambient temperature.The broad range of substrates includes aromatic, heteroaromatic, aliphatic, and cyclic aldehydes used to dimerize aldehydes.In general, the activity of complex 31 was either identical to or slightly better than that of complex 32.Aromatic aldehydes containing electron-donating groups react faster than those containing electron-withdrawing groups.The most active substrates were found to be cyclic or branched aliphatic aldehydes.The yield of the product depended on the position of the substituent on the phenyl ring.The substrates that interact with the highly electrophilic thorium catalyst exhibited a decrease in reactivity, restricting the coupling of the aldehyde and the metal-alkoxo moiety.When complex 31 was employed to perform the cross-Tishchenko reaction of benzaldehyde and 1-naphthaldehyde, all four potential ester products formed as expected (Table 7).However, the reaction initially preferred the formation of an unsymmetrical ester (3) over symmetrical ones (1 and 2).Over time, the reaction shied towards symmetrical esters, with the other unsymmetrical ester (4) becoming nearly undetectable.Chemoselective ester (3) formation was achieved by using a ratio of 1.5 : 1 of the aldehyde (RCHO : R 0 CHO) in the reaction mixture.A cross-Tishchenko reaction of benzaldehyde and pyridine-2-carbaldehyde in a 1 : 1 ratio yielded four different types of esters, with ester (3) dominating.This selectivity towards ester (3) was attributed to the increased benzaldehyde-to-pyridine-2-carbaldehyde ratio (1.5 : 1).The selectivity of this reaction was likely attributed to the hydride acceptor and donor characteristics of the aldehydes.The cross-Tishchenko reaction of benzaldehyde with aliphatic aldehydes (cyclohexanecarboxaldehyde, isobutyraldehyde) produced a negligible ester (3).Whereas, aliphatic aldehydes preferentially donate hydride, favoring esters (2) and (4).Poisoning experiments were also performed using the equimolar amount of isopropanol and a catalyst 31 demonstrated that increasing the proportion of isopropanol from 0.25 to 0.5, showed a decline in the catalytic activity from 25% to 50%, suggesting that all methyl groups were active in the catalytic cycle.Kinetic studies of the initial rates of the reaction with complex 31 and 32 determined that the reaction follows a rstorder dependence for aldehyde and complex.Therefore, an apparent rate law for the dimerization of aldehyde promoted by precatalysts 31 and 32 can be expressed as indicated in eqn (3).
A primary kinetic isotopic effect of 2.7 was measured when the reaction was studied with a-deuterated benzaldehyde.This study revealed that hydride transfer was involved in a rate-determining step.According to thermodynamic studies, the energy of activation (E a ), enthalpy of activation (DH ‡ ), and entropy of activation (DS ‡ ) were 3.48 kcal mol −1 , 2.63 kcal mol −1 , and −68.4 eu, respectively.The signicantly negative value of entropy at the RDS indicated a well-ordered transition state.Scheme 19 depicts a plausible mechanism for the dimerization of aldehydes by complex 31. 102In the rst step of the reaction, an aldehyde was rapidly inserted into the Th-CH 3 bond using a four-centered transition state to form the thorium alkoxo intermediate (F 1 ).When a second aldehyde was introduced into the Th-O bond, an intermediate (F 2 ) was formed.Subsequent hydride transfer to an incoming aldehyde via a chair-like six-membered transition state (F 3 ) produced the catalytically active intermediate (F 4 ) and one equivalent of the methylated ester.The addition of an aldehyde to the Th-O bond of the intermediate (F 4 ) led to the formation of the intermediate complex (F 5 ), which aer undergoing a hydride transfer reaction (step 5, RDS) with an additional aldehyde, brought the catalytic cycle to an end to give the product (1) and regenerated the active complex (F 4 ).

Ethyllanthanoid iodide complex catalyzed Tishchenko reaction
1][132][133][134][135] The catalysts 33a-33c were synthesized from the reaction between lanthanide metal (Ln = Pr, Nd, Sm) and ethyl iodide.In the presence of catalysts 33a-33c, arylic and aliphatic aldehydes were shown to undergo Tishchenko reactions with identical catalytic activity.2][133][134][135] Even though divalent lanthanide species like Yb and Eu demonstrated catalytic activity for the Tishchenko reaction, the yield was lower.Despite the prevalence of aluminum alkoxides, 28,136,137 as catalysts for the Tishchenko reaction, the lanthanide-based investigation revealed the potential of compounds 33a-33c as alternative catalytic precursors for the Tishchenko reaction.
The mechanism was shown in Scheme 20, which was similar to that of the reaction with the aluminum alkoxides. 103The rst step was the elimination of the ethylene molecule from 33 to generate the active catalyst (G 1 ).The formation of the lanthanide-alkoxide complex PhCH 2 O-LnX 2 (G 2 ), was achieved by bhydride elimination, through an additional reaction between (G 1 ) and benzaldehyde.Aer which the second molecule of benzaldehyde was added to afford an intermediate (G 3 ).Again, the addition of benzaldehyde to intermediate (G 3 ) afforded the corresponding ester and (G 1 ).Despite the tungsten-promoted Tishchenko reaction was already reported, this was the rst example of a lanthanide-catalyzed Tishchenko condensation of aldehydes.
Ishii et al. have found that 5 (ref.48) acts as an active catalyst for the transformation of benzaldehyde into benzyl benzoate.In comparison to transition metal catalysts like 5 and 6, 49 the activity of the lanthanocene complexes (34a-34b) was higher.Furfural dimerization was extremely difficult in the presence of 34 or 7 catalysts. 50The use of 7 in combination with crown ethers as a catalyst resulted in the production of esters with good yield. 50,136,139Only aliphatic aldehydes with branching acarbon (pivalaldehyde and cyclohexanecarboxaldehyde) produced the corresponding dimers in good yield whereas the aldehydes without a-branching afforded dehydrated trimers as the major product.The catalyst 34b was more active than commercial La(OCHMe 2 ) 3 (35), 104 which was very sensitive to the structure of the substrate.It has been noted that the esters were formed in good yield when p-substituted benzaldehydes were used as a substrate.The activity of aromatic aldehydes was improved by incorporating electron-withdrawing substituents in the para position.The yield trend of p-substituted benzaldehydes was expressed as follows: MeO < Me < Cl < NC.The Tishchenko reaction of dialdehyde was studied using o-phthalaldehyde.The reaction of o-phthalaldehyde in the presence of catalyst 34a afforded phthalide in good yield (Scheme 22).The GC-MS analysis revealed that the intermolecular dimerization product was not formed during this reaction.The presence of catalyst 34b led to the formation of oligomers (M w = 300) and polymers (M w = 6300) as a result of the reaction of isophthalaldehyde, with the latter being the predominant product (Scheme 23).When the reaction mixture was heated, the molecular weight of the polymer increased but the quantity of the polymer was decreased.Aer prolonged heating, the oligomers were formed as a major product.The transformation of the polymer into a thermodynamically stable oligoester indicated the occurrence of an ester exchange reaction in the presence of 34b.
The formed oligomers contain two isomers (H 1 ) and (H 2 ).The structures of oligomers were possibly to be cyclic triesters of isophthalaldehyde.This was conrmed by the absence of an aldehydic proton signal in 1 H NMR analysis.The three (1 : 1 : 1) methylene signals and three (1 : 1 : 1) carbonyl signals of the 13 C NMR spectrum show that the main isomer (H 1 ) has an irregular structure.The reaction of terephthalaldehyde in the presence of catalyst 34a afforded the corresponding polymer in good yield (Scheme 24).In this reaction, there was no intramolecular dimerization and oligomerization (like ortho and meta isomer respectively) observed.It was found that the molecular weight of the polymer increased as the reaction time increased.The polymer's irregular structure resulted from the presence of two signals in the 1 H NMR and three methylene signals in the 13 C NMR spectrum, indicating its complex composition.
The process involving the polymerization of di(4formylphenyl)ether afforded the corresponding polymer with high molecular weight (Scheme 25).The mechanism of the Tishchenko reaction was briey explained in Scheme 26. 104omplex 34b reacted with benzaldehyde to afford alkoxo complex (H 3 ).The formation of (H 3 ) was conrmed by new mutually coupled doublets at d 0.94 ppm (methine proton attached to two silicon atoms) and at d 5.33 ppm (benzylic proton) in the 1 H NMR spectrum.The complex (H 3 ) was treated with an excess of benzaldehyde to produce benzyl benzoate, ketone (H 4 ), and pentamethylcyclopetadienyl phenyl ketone (H 5 ).In the 1 H NMR spectrum, the signal at d 6.9 ppm (broad) indicated the formation of PhCH 2 OLa species with corresponding ketones.The formed PhCH 2 OLa species was conrmed by the addition of a large amount of chlorotrimethyl silane to the former mixture which resulted in the production of trimethylsilyl benzyl ether.As a result, benzyloxy-La was iden-tied as the active species during the Tishchenko reaction.
Scheme 27 depicts the catalytic cycle and its mechanism. 104he rst step in the catalytic cycle involved the aldehyde insertion into the Ln-OR bond, resulting in the formation of hemiacetal-Ln species (H 9 ).Aer the formation of (H 9 ), there were two different pathways.In pathway A, an aldehyde was coordinated to a metal ion (H 9 ), and the hydride subsequently migrated through a six-membered transition state and led to the formation of a product.Path B proceeds with direct bhydride elimination from (H 9 ) forming Ln-H species followed by aldehyde insertion.

Lanthanide amides catalyzed Tishchenko reaction
Berberich and co-workers reported the lanthanide-supported bis(trimethylsilyl)amides, M[N(SiMe 3 ) 2 ] 3 (36) [M = La (36a), Sm (36b)] as an efficient catalyst for Tishchenko reactions. 6,105he discovery of compound 36 has resulted in numerous advances in lanthanide chemistry.The compound 36 was recognized as a well-known starting material for lanthanide metals through the easy cleavage of the silylamide group in the past 100 years.A comparison of 36a with 36b showed that 36a displayed good catalytic activity with higher turnover frequency (TOF-87) than 36b (TOF-80).The TOF was proportional to the ionic size of the central metal atom.A comparison with other Tishchenko catalysts such as boric acid (37), 140  (35), 104 SmI 2 (38), 42 and [Sm{O-2,6-( t Bu) 2 -C 6 H 3 } 3 ] (39) 141 showed that complex 37 needed extreme reaction conditions whereas 35 and 38 were inert in the case of benzaldehyde and 39 displayed some catalytic activity but lower than 36a and 36b. 18In the Tishchenko reaction, Onozawa et al. described the application of the 34b complex as an active catalyst. 104Although the catalytic activity of 34b was lower, it competes with 36a (yield: 98% (36a), 88% (34b)).The catalyst 34b was most likely to yield the same active species as 36a, although it was much more difficult to prepare.The mechanism of the Tishchenko reaction was elucidated was followed by hydride migration to produce (H 13 ) (Scheme 28) which further eliminated ester (1) and regenerated the (H 10 ).Catalytic and stoichiometric analyses of 36b revealed that all amide groups were eliminated without taking a signicant reaction time.The 1 H NMR spectrum revealed that the signals were associated with SmOCH 2 groups.The catalytically active species 36a was believed to yield the same or a comparable product as 34b in a Tishchenko reaction.The following observations agree with this statement: (i) both the catalysts 36a and 34b produced similar yields, and (ii) both catalysts can interchange their original ligand shells during the process.43) which can acts as catalyst for the Tishchenko reaction. 18The complexes 41 and 42 were synthesized by the reaction of 3,5-di-tert-butylpyrazole ( t Bu 2 pzH) with corresponding metal in the presence of mercury without any particular solvent (Scheme 29).
Usually, the Al(OR) 3 (44) 28,136 were commonly used as a catalyst for the Tishchenko reaction.Instead of 44, the compound 41a can be used as a catalyst for Tishchenko reaction.The catalytic activities of compound 36a were compared to those of the highly active silylamide catalyst 41a by using a range of aliphatic aldehydes and substituted benzaldehydes.The highest production of benzyl benzoate was achieved when compound 41a was utilized while using 36a resulted in moderate yields. 105The product yield was higher for compound 41a than the high-speed aluminum catalysts such as [2,7dimethyl-1,8-biphenyldioxy-bis(diisopropoxy aluminum(III))] (44a) and [2,7-dimethyl-1,8-biphenyldioxy-bis(dibenzyloxy aluminum(III))] (44b). 142,143Substrates such as aliphatic aldehydes and o-phthalaldehydes showed impressive quantitative yields and remarkably high TOFs when reacted with 41a, which can be compared to the results obtained with 36a.Para-substituted benzaldehydes were employed as substrates to determine the tolerance of 41a to functional groups.When the halogen atom was substituted to the para position of the benzaldehyde substrate, yields were slightly reduced.The Tishchenko reaction does not take place when the substrate contains heteroatoms such as O and S.This was because the coordination of O and S to the catalyst hinders its catalytic activity.While comparing the TOFs of benzaldehyde and substituted benzaldehydes using catalyst 41a, the latter was lower than the former.The lower reactivity of 41a than 36a was mainly due to the structural and steric factors.Complex 41a exists as a dimer in benzene-d 6 .Aer that, it comes into contact with the reaction solvent, and substrate induction, 41a dissociated into a monomer, which was a key step in the catalytic process.Although the preparation of the catalysts 41-42 was easy, these catalysts displayed less catalytic activity as compared to lanthanocene complexes.
1 H NMR study indicated the formation of benzyl benzoate through an increase in the benzyl proton signal and a corresponding decrease in the aldehydic proton signal.When benzaldehyde undergoes a reaction with compound 45 in a 5 : 1 ratio, the formamidinate ligand is partially cleaved off.From the comparison of compounds 45-47, 45 exhibited a turnover of 200 h −1 with 99% yield within 0.5 h and possessed the highest catalytic activity.The extreme activity was a result of the smallest formamidinate ligands (which are more readily attacked by the aldehyde, hence accelerating the initial conversion), two labile THF groups, and less steric hindrance of complex 45.and B(OH) 3 (49), 140 etc., also failed to catalyze this reaction whereas some transition metal catalysts like amino alcohol-based iridium bifunctional catalyst 146 gave high yields (86%) but were slower than lanthanum catalysts.Compound 45 was the best catalyst for the Tishchenko reaction rather than above mentioned catalysts.Aromatic aldehydes such as o-phthalaldehyde undergo intramolecular Tishchenko reaction giving high yields (quantitative) and high TOF (>1500 h −1 ).Even when utilizing 7/crown ether, the heteroaromatic aldehyde-like furfural exhibited little reactivity, and only a yield of 3.4% was achieved. 50,136,139In contrast, lanthanum catalysts enhanced their activity and produced much higher yields (relative to 7).Cyclic and non-cyclic aldehydes also play the role of substrates in the Tishchenko reaction.Catalysts 45-47 were slower to the Tischenko reaction of pivalaldehyde, because of the steric bulk of the starting material.And nally, it concluded that catalysts 45-47 were superior to all the catalysts discussed above.Compound 45 was able to catalyze quickly and gave high yields for aldehyde substrate with or without a-hydrogen.Butanol, when subjected to a temperature of 21 °C, generates higher coupling products such as butyl butyrate, trimeric, and tetrameric coupling products. 28,137,147,1480][151][152][153][154][155] The extremely high activity of the catalysts 45 to 47 was attributable to the following factors: (i) Lewis acidity and (ii) ligand sphere interchangeability.These are the most active catalysts ever recorded for the Tishchenko reaction.The catalytic activity increased in the following order: 45 > 46 > 47.
Recently, Salehisaki et al. revealed the synthesis and applications of PhForm complexes as Tishchenko reaction catalysts. 107These complexes had much lower activity as compared to the known benchmark catalyst, [La(O-Tol-Form) 3 (THF) 2 ] (45).Surprisingly, the yttrium complex from the PhForm series displayed excellent catalytic performance, contradicting previous results about lanthanide size trends.Further investigation of DMForm complexes indicated even lower activity, except [Y(DMForm) 3 (THF)] (50), which remarkably outperformed all other catalysts studied.The anionic complexes Eu (51c) and Nd (51d), as well as the neutral complex (52a-52b), were made by metathesis of the appropriate chloride with the lithium salt (Scheme 31). 156To examine the catalytic behavior of these catalysts, the Tishchenko reaction was carried out using benzaldehyde as a substrate.Unexpectedly, yields of ester were obtained aer 3 hours of reaction and were found to be 37% for 51 and 25% for 52.This suggested that the catalyst used in this method was less efficient than the already reported homoleptic lanthanide amide catalyst 36. 105Although 51 and 52 were used as good catalysts in the amidation reaction, these catalysts failed to be efficient catalysts in the Tishchenko reaction.

Cationic lanthanide complex catalyzed Tishchenko reaction
Guevara-Pulido and colleagues gained attention for their successful one-pot synthesis of enantioenriched trisubstituted lactones, which was accomplished using a one-pot process involving sequential organocatalyzed Michael addition of ketones to enals, followed by catalytic intramolecular diastereoselective Tishchenko reaction and lactonization. 157Notably, the end product was a single diastereoisomer, showing that any combination of anti and syn diastereomers converted to syn hydroxy ester during the process.A novel approach was developed to produce trisubstituted d-lactone from ketone and aldehyde in a single step (Scheme 32).This novel strategy decreases the requirement for purication steps, minimizes waste chemical formation, and shortens overall reaction time, increasing overall yield.In their approach, a combination of ketone (I) (1.2 equiv.),aldehyde (II) (1 equiv.),prolinol derivative A (0.1 equiv.)as a catalyst, and PNBA (0.5 equiv.)as a co-catalyst in 2-propanol was stirred at 0 °C until the reaction was complete.Following that, Yb(OTf) 3 (53) (0.1 equiv.) was added to the mixture, which was heated until (III) vanished.Aer extracting the 2-propanol under vacuum, the residue was dissolved in benzene and heated until (IV) was no longer detectable giving a good yield of trisubstituted d-lactone (V).Scheme 33 describes the stereochemical outcome of the Tishchenko reaction.When a metal was coordinated to both carbonyl groups, it formed a mixture of active diastereomeric complexes (C) and (D).These complexes immediately isomerize to the most stable complex (D), as both substituents were equatorial.The addition of i-PrOH to the 5-oxopentanal-derived complex (D) took place on the exterior less hindered Re-face of the formyl group, resulting in a chelated hemiacetal complex (E).The stereochemistry at C-5 in the hydroxy ester (IV), produced as a single diastereoisomer, was determined via intramolecular hydride transfer across a six-membered concerted transition state (F).The nal lactones (V) were produced by changing the solvent and then cyclizing (IV).
The approach performs effectively with benzyl ketones and ketosulfones as nucleophiles, and b-substituted alkyl-and arylenals as electrophiles.It must be emphasised that the transformation of anti to syn diastereoisomers, which began with the rst Michael addition, occurs throughout the oxido-reduction step, separating lactones as the solitary diastereoisomer.This entire process is carried out in one pot, resulting in less waste, time, and no need for purication procedures.
In order to compare the catalytic activity, the benzaldehydebenzyl benzoate reaction was used as a model reaction.For catalysts 54a and 54b, a conversion of benzaldehyde was 31 and 57 equivalents respectively.Aer the separation of the supernatant, no activity was seen aer 15 h of benzaldehyde addition.It indicated that the active species exists on the surface of silica.For trisamido catalysts, 36b and 36c the conversion of aldehydes was higher 89% and 67% respectively.It showed that supported catalysts were found to be less efficient than unsupported ones (36b and 36c) under the same reaction conditions.The yield reached a plateau aer 6 h with graed catalysts 54a and 54b.This was due to the inhibition process of the product formed by the reaction.This behavior of the catalysts was attributed to the distinct natures of the active sites.In homogeneous lanthanide clusters, benzylato ligands were small to form monomeric complexes, 158 whereas surface lanthanide alkoxides were mononuclear in graed catalysts.Aer 3 hours of reaction time, the supernatant was removed from the solid catalyst.The reaction-modied silica was rinsed with toluene, and then a fresh substrate was added to the solution.Conversion by the rst run was 38% whereas the second and third run was 16% and 15% respectively.The catalytic activity of 54 was low compared to 36.55) is an efficient and mild catalyst for the Tishchenko reaction that converts benzaldehyde to benzyl benzoate. 110Compound 55 was prepared using the immobilization method.][161][162] By comparing the catalysts 36b and 55, the reaction rate of heterogeneous catalyst 55 was somewhat slower than homogeneous catalyst 36b, because of the restricted diffusion.Under the same experimental conditions yields were also lower than the corresponding homogeneous catalyst 36b.However, the overall yield of 55 was comparable with the homogeneous catalyst with prolonged reaction time.In the case of substituted aldehydes, low yields were obtained as a result of the steric hindrance and the +M effect of the substituent on the phenyl ring.If butyl aldehyde was used as a substrate with 55 as a catalyst, different product selectivity could be achieved rather than a homogeneous 36b catalyst.Trimers and oligomers were obtained while using 55 and 36b respectively (Scheme 36).The difference between the above was the pore connement of hybrid material, which did not allow the trimeric substance to undergo further aggregation with other aldehydes.Catalyst 55 showed higher stability towards oxygen than 36b.This implied that by utilizing 55 as a catalyst, the reaction can be carried out without the need for N 2 protection, which was not achievable with 36b.The catalyst 55 can be removed easily from the reaction mixture and reused.In many cases recovered material showed inherent activity while using subsequent runs.However, X-ray diffraction and N 2 sorption examination demonstrated that the recovered material possesses the same pore size and well-ordered microstructure as 55.These ndings indicated that there was no obstruction of pores in 55 during the whole catalytic process, perhaps because of the signicant pore width and volume of SBA-15.The elemental analyses and IR studies suggested that silylamide ligands were replaced by formed alkoxide ligands. 104To investigate the catalytic performance of hybrid catalyst 55, the mixed Tishchenko reaction was conducted (Scheme 37).When various types of aldehydes were combined in equal proportions (1 : 1) with hybrid catalyst 55, the formation of the resulting cross-products was greater compared to the homogeneous catalysts.This selectivity resulted from the spatial restriction and diffusion control of the surface connement of the hybrid solid material.1 mol% of 56b at room temperature for approximately 2 hours afforded 78% yield of the corresponding ester.The catalytic activities of all the lanthanide heterometal clusters 56a-56e were tested and all gave good yields.Compound 56a exhibited superior activity with a 93% isolated yield, while 56d displayed the lowest yield and lower activity.In the cases of NaOCH 2 -CH 2 NMe 2 (57), there was no reaction, which means that benzaldehyde did not undergo a Tishchenko reaction without the lanthanide complex.Despite being a lanthanide complex, Nd(OCH 2 CH 2 NMe 2 ) (58) was inactive for the Tishchenko reaction.56b has a catalytic activity that rivals other high-speed catalysts, such as 44a and 44b 142 in the Tishchenko reaction.The activity of 56b exceeded that of 35, 6,104 38, 6,105 and 39 (ref.6)  but was lower than 36.The only benet of 56b was its reduced susceptibility to air and moisture.Several kinds of aromatic, heteroaromatic, and aliphatic aldehydes were examined with 56b.All reactions were smoothly taking place with 1 mol% of 56b except for 2-furaldehyde (39% yield) afforded moderate to higher yields.The lower yield of 2-furaldehyde resulted from the coordination of each oxygen in the ether to the lanthanide metal, which resulted in the formation of a stable vemembered metallocycle that partially inhibits the active species.This was the same situation as with lanthanide silylamide complexes. 6,105olerance of 56b was tested with different types of parasubstituted benzaldehyde substrates.According to the results, cluster 56b was very tolerant to functional groups, and a higher yield was produced when the aromatic ring contained an electron-donating substituent.This was due to the coordination of metal with the carbonyl group.Ultimately, it was discovered that heterometal alkoxide clusters 56a-56e outperformed previously documented lanthanide silylamide catalysts in the Tishchenko reaction.This was attributed to their enhanced ability to withstand a wide range of functional groups.This outcome could be attributed to the cooperation between the lanthanide and sodium centers.Various types of lanthanide catalysts and their catalytic activities, yield, and TOFs are described in Table 8.

Lanthanide heterometal clusters catalyzed Tishchenko reaction
The Tishchenko reaction involves the conversion of different types of aldehyde substrates, including aromatic, heteroaromatic, and aliphatic aldehydes, into corresponding esters.This transformation is facilitated by the use of various lanthanide complexes (33-56) as catalysts, as shown in Table 9.

Conclusion
This review meticulously examines actinide and lanthanide complexes as potential Tishchenko reaction catalysts.Their advantages, including high yields, broad substrate scope, and tolerance to functional groups, identify them as strong contenders for future dominance in Tishchenko applications.Employing specically designed ligands and optimized reaction conditions can circumvent challenges encountered during the Tishchenko reaction, enabling organoactinide and organolanthanide complexes to excel as powerful catalysts for the esterication of aldehydes.Ligand design, specically tuning their steric and electronic features, is a key strategy for optimizing the catalytic activity and selectivity of organoactinide and organolanthanide complexes.The ligands imidazolin-2-imine, benzimidazolin-2-imine, and perimidin-2imine have shown remarkable activity and selectivity in the Tishchenko reaction, and have emerged as extremely effective scaffolds for organoactinide catalysts.The Tishchenko reaction mechanism with organoactinide catalysts involves many phases, including aldehyde insertion into the metal-carbon bond, rate-determining hydride transfer, and ester elimination.Lanthanide catalysts also perform a similar Tishchenko reaction, involving aldehyde insertion, hydride migration, and alkoxide transfer.
The mechanism of the Tishchenko reaction with actinide and lanthanide catalysts is still not fully understood.Further research is required to determine the precise functions of the actinide and lanthanide metals, as well as the ligands, in the catalytic cycle.Understanding the mechanism allows for more efficient catalyst design.The strategic application of organoactinide and organolanthanide complexes offers novel opportunities for the utilization of actinides and lanthanides in organic synthesis.The use of specically designed ligand designs and reaction conditions can enable the synthesis of more active organoactinide and organolanthanide catalysts.The Tishchenko reaction is still being researched, and new actinide and lanthanide-based catalysts are being synthesized all the time.It would be fascinating to examine how the catalysts detailed here compare to the most recent breakthroughs in the eld.

a
Scheme 19Proposed mechanism for the Tishchenko reaction mediated by complex 31.

Scheme 27
Scheme 27 Catalytic cycle for the Tishchenko reaction.

40 a
Conversion in NMR scale.b Trimers and tetramers were produced as a by-product determined by GC-MS.

Table 2
Dimerization of aldehydes by thorium complexes

Table 1
Thermodynamic data of substituted and unsubstituted benzaldehyde during the Tishchenko reaction with precatalyst 10SubstrateE a (kcal mol −1 ) DH ‡ (kcal mol −1 ) DS ‡ (eu) Scheme 9 A plausible mechanism for the catalytic dimerization of aldehyde by organoactinide complex 10.

Table 9
Results for the dimerization of various aldehydes using different lanthanide catalysts