Catalytic, Kinetic, and Mechanistic Insights into the Fixation of CO2 with Epoxides Catalyzed by Phenol‐Functionalized Phosphonium Salts

Abstract A series of hydroxy‐functionalized phosphonium salts were studied as bifunctional catalysts for the conversion of CO2 with epoxides under mild and solvent‐free conditions. The reaction in the presence of a phenol‐based phosphonium iodide proceeded via a first order rection kinetic with respect to the substrate. Notably, in contrast to the aliphatic analogue, the phenol‐based catalyst showed no product inhibition. The temperature dependence of the reaction rate was investigated, and the activation energy for the model reaction was determined from an Arrhenius‐plot (E a=39.6 kJ mol−1). The substrate scope was also evaluated. Under the optimized reaction conditions, 20 terminal epoxides were converted at room temperature to the corresponding cyclic carbonates, which were isolated in yields up to 99 %. The reaction is easily scalable and was performed on a scale up to 50 g substrate. Moreover, this method was applied in the synthesis of the antitussive agent dropropizine starting from epichlorohydrin and phenylpiperazine. Furthermore, DFT calculations were performed to rationalize the mechanism and the high efficiency of the phenol‐based phosphonium iodide catalyst. The calculation confirmed the activation of the epoxide via hydrogen bonding for the iodide salt, which facilitates the ring‐opening step. Notably, the effective Gibbs energy barrier regarding this step is 97 kJ mol−1 for the bromide and 72 kJ mol−1 for the iodide salt, which explains the difference in activity.


Introduction
The use of CO 2 as a C 1 building block is receiving increasing attention from the scientific and industrial community due to economic and ecological considerations. [1] It is progressively regarded as an attractive, inexpensive, and abundant renewable feedstock rather than waste. [2] Furthermore, in a future CO 2 based circular economy it can be used as a platform to produce bulk chemicals and energy carriers through its transformation to fuels. [3] Nevertheless, due to its thermodynamic stability, the efficient activation and chemical fixation is still challenging. [4] This can be partially overcome by converting CO 2 with highenergy starting materials such as epoxides or hydrogen in the presence of a catalyst. Thus, it is crucial to develop new catalytic processes that allow the efficient transformation of CO 2 into valuable products. Promising transformations even on an industrial scale are the fixation of CO 2 into organic carbonates or polycarbonates (Scheme 1, A). [1b,5] These processes can be of significant advantage regarding economic and ecological considerations, for example, by saving fossil resources or lowering the carbon footprint of a process. [6] The synthesis of five-membered cyclic carbonates 2 from CO 2 and epoxides 1 is of particular interest. It is an atomeconomic reaction and an excellent example of green chemistry. [7] Moreover, cyclic carbonates are important materials that are used in various applications, for example, as intermediates in organic synthesis, [8] indirect CO 2 reductions to methanol, [9] green solvents, [10] electrolyte in lithium ion batteries, [11] polymer building blocks, [12] and even as additives in drugs and cosmetics. [13] Metal-based systems including Al-salen [14] and triphenolat [15] complexes have been reported for the synthesis of cyclic carbonates. [16] In these binary catalytic systems, the Lewis-acidic metal complexes are often combined with an external nucleophile, typically a halide ion from an onium salt, to activate the epoxide (Scheme 1, B). The nucleophilic counter anion of the salt acts as a temporary relay, ring-opening the epoxide, which is activated by the Lewis-acidic metal center, and subsequently serving as a leaving group upon ring closure after CO 2 insertion. Catalytic systems that operate under nearambient conditions (low CO 2 pressure and room temperature) are of interest in terms of advances towards sustainability. [17] In the past decade, the use of organocatalysts has attracted increasing attention in this research area. [18] A significant benefit of this catalyst class is undoubtedly the metal-free carbonbased scaffold, which is associated with a high potential for structural modification, catalyst tuning, and immobilization. [19] In analogy to the metal-based systems, the combination of hydrogen bond donors and quaternary ammonium salts to activate the epoxide proved to be a promising concept in the field of organocatalyzed cyclic carbonate synthesis (Scheme 1, B). [20] Systems based on different hydrogen bond donor functionalities, such as alcohols, [21] carboxylic acids, [22] silanol, [23] phenols, [24] and (thio-)ureas, [25] were used in combination with external nucleophiles to catalyze the addition of CO 2 to epoxides to yield the corresponding cyclic carbonates. Even though great advances have been made it is still challenging to realize this reaction efficiently under low CO 2 pressures (1 atm) and reaction temperatures below 100°C. [17] It is generally recognized that bifunctional catalysts consisting of an electrophilic group and an internal nucleophile significantly accelerate the process through synergistic effects. [18,26] However, it was not until recently that bifunctional phosphonium salts emerged as potent class of organocatalysts (Scheme 1, C). In 2014 our group reported the use of bifunctional phosphonium salt catalyst 3 bearing an alcohol moiety as hydrogen bond donor. This catalyst allowed for the synthesis of cyclic carbonates at 90°C and 1.0 MPa CO 2 pressure, yielding the desired products in up to 99 % yield under solvent-free conditions. [27] More recently, we reported a mechanistic study on the use of bifunctional phosphonium salt 3. [26a] This study clearly showed that the epoxide is activated by hydrogen bonding and that the order of reactivity in regard to the anion increased in the order Cl À < Br À < I À . Significantly, the analysis of the kinetic data revealed that partial product inhibition hampered the overall efficiency of this catalyst. Also in 2014, Wei-Li et al. introduced carboxylic acid derivative 4 as a catalyst for the synthesis of cyclic carbonates at elevated temperatures and pressure (130°C and 2.5 MPa). [28] In 2016, Liu et al. showed that biphenyl-derived phosphonium salt 5 enables the conversion of epoxides with CO 2 at 60°C and low CO 2 pressure (1.0 atm). [29] In the same year, Toda et al. studied bifunctional tetraarylphosphonium salt 6, which allowed for the synthesis of cyclic carbonate at atmospheric CO 2 pressure but high reaction temperatures of 120°C in chlorobenzene as the solvent. [30] Very recently, they carefully investigated the impact of the electronic properties of the substituents on the catalyst efficiency. [31] The introduction of electron-donating groups significantly enhanced the catalytic activity, which allowed to reduce the reaction temperature to 60°C. In 2017 our group reported the use of bifunctional phenolic phosphonium bromide 7 for the preparation of oleochemical carbonates at 80°C and 2.5 MPa CO 2 pressure. [32] Based on our previous results we envisioned that the corresponding iodide 8 should show superior efficiency as catalyst in the synthesis of cyclic carbonates under mild and solvent free-conditions. Herein we report the synthesis and application of this catalyst as well as thorough kinetic investigations and DFT calculations to rationalize its superior performance and the reaction mechanism.

Catalyst screening
We chose the conversion of 1,2-butylene oxide (1 a) with CO 2 to produce 1,2-butylene carbonate (2 a) as a benchmark system to evaluate and compare to previously reported catalysts under uniform reaction conditions (Table 1). Our first-generation bifunctional phosphonium salt 3 (2 mol %) gave the desired product 2 a in 25 % yield after 24 h at 23°C and 1.0 MPa CO 2 pressure (Table 1, entry 1). In the presence of catalysts 5, 6, and 7 significantly lower conversions and yields � 10 % were achieved (entries 2-4). In contrast, phosphonium iodide 8 gave 2 a in 65 % yield (entry 5). This is remarkable since catalyst 7 was identified to be more efficient compared to 8 at higher temperature (100°C) and CO 2 pressure (5.0 MPa) in the synthesis of oleochemical carbonates. [32] With increasing reaction temperature the obtained yield for 2 a equalizes (entries 6-9). Notably, in the presence of 5 mol % 8 an excellent yield > 99 % was achieved at 23°C (entry 10). Even at a lower CO 2 pressure of 0.1 MPa 2 a was obtained in 71 % yield (entry 11). The lower yield might be due to a lower CO 2 concentration in solution at this pressure, which can have a strong impact on the reaction rate. [33] Scheme 1. Synthesis of cyclic and polycarbonates as well as concepts and selected catalysts for the conversion of epoxides with CO 2 .

Kinetic investigations
The efficiency of bifunctional phosphonium salts is closely related to the ability of activating the epoxide by hydrogen bonding. [20] Recently, we reported a detailed mechanistic study on alkyl-bridged bifunctional phosphonium salts as catalysts in cyclic carbonate synthesis. [26a] In this study the activation of epoxide 1 a by hydrogen bonding to catalyst 3 was proven by IR spectroscopy. Moreover, kinetic and IR studies revealed an interaction of 3 with the product 2 a leading to significant product inhibition. In the present case attempts failed to investigate the interaction of phenolic catalyst 8 with the epoxide or the carbonate by transmission IR spectroscopy due to an overlap of the OH-stretching vibration from the phenol moiety with bands of the CÀ H stretching modes. Unfortunately, also measurements in the attenuated total reflection (ATR) mode did not provide unambiguous results in this regard. [34] However, to further investigate the difference in the activity of catalysts 3 and 8, we performed kinetic measurements of the model reaction with 1,2-butylene oxide (1 a) as the substrate at 23 and 45°C. These experiments have been conducted at a CO 2 pressure of 1.0 MPa with a substrate content of 460 mmol and 2 mol % of catalyst. Product formation was monitored by the sampling of the liquid reaction mixture at distinct time intervals followed by 1 H NMR spectroscopic analyses. The selectivity of 2 a was consistently > 99 %. At 23°C with 8 as a catalyst, an induction period was observed, which was attributed to the low solubility of 8 in the pure epoxide at room temperature. [34] For the catalyst system 3, no induction period has been identified, but at higher conversions the catalytic performance is significantly lower compared to the phenolic catalyst 8. In the next step, we performed these model reactions at 45°C. Now, for the catalyst 8, the yield versus time data can be described by a firstorder kinetic model [Eq. (1)], in which Y is the yield and k obs is the observable rate constant, as shown in Figure 1.
In contrast, for the reaction in the presence of 3 a kinetic model in which product inhibition was considered needs to be used [Eq. (2)]. This equation is based on a Michaelis-Menten model including a reversible product inhibition, which is valid for the case of a first order with respect to the substrate. The equilibrium constant K inh of the product inhibition with the aliphatic catalyst 3 was calculated as 0.260 L mol À 1 for the given initial substrate concentration [S] 0 . The fact that the yield versus time data for 8 was best described with the first-order model indicates that product inhibition is not relevant for this system. The obtained observable rate constants k obs were 0.197 h À 1 (8) > 0.0605 h À 1 (3), reflecting the catalytic activity. [34] From these observations it can be concluded that both the absence of a significant product inhibition and an intrinsically higher activity for the catalytic system with catalyst 8 cause its better performance.
We were further interested in the temperature dependence of the reaction rate for the catalytic system with the phenolic catalyst 8. [34] Therefore, additional experiments have been performed so that a temperature range of 35-90°C was covered. Yield versus time data was analyzed using a first-order kinetic model (first-order with respect to the substrate concentration) providing observable rate constants (k obs ). An acceptable Arrhenius behavior was found between 35-65°C (T = 308.15-338.15 K). Interestingly, at higher temperatures the values of the rate constant decreased, which might be attributed to a change in the solubility of CO 2 at higher temperatures. [33b] From an Arrhenius-plot a value for the activation energy was calculated with E a = 39.6 kJ mol À 1 , which is in agreement with previous reports (Figure 2). [35] A respective Eyring-plot allowed for the calculation of the enthalpy of activation, which gave a value of ΔH � = 36.9 kJ mol À 1 .  [b] 8 5 23 24 71 36 Reaction conditions: 1.0 equiv. 1 a (1.00 g, 13.9 mmol), 2-5 mol % catalyst, 2-24 h, p(CO 2 ) = 1.0 MPa, solvent-free.

Substrate scope
Due to the observed superior efficiency of catalyst 8 we evaluated the substrate scope regarding the conversion of terminal epoxides 1 to the respective cyclic carbonates 2 at room temperature ( Figure 3). Carbonates 2 a-d bearing aliphatic substituents were synthesized in good to excellent yields. Particularly, propylene carbonate (2 b) has attracted much interest due to its applications as an electrolyte in lithium-ion batteries [11] and is regarded as one of the most sustainable alternative solvents in organic chemistry. [10a] Notably, the conversion of enantiomerically pure (S)-propylene oxide (S-1 b) led to the corresponding cyclic carbonates S-2 b in 94 % yield and > 99 % enantiomeric excess (ee). Due to the lower polarity of epoxides 1 c and 1 d the solubility of the catalyst was reduced, and the addition of a solvent (nBuOH) was required to achieve 95 and 72 % yield for 2 c and 2 d, respectively. The phenyl-substituted product 2 e was isolated in a yield of 74 %. In this case acetophenone was found as a by-product that was derived from a Meinwald rearrangement. [36] This indicates that the conversion of styrene oxide (1 e) proceeds at least partially via a cationic intermediate. This assumption is supported by the partial racemization, which was observed when (R)-styrene oxide (R-1 e) was converted. In this case, carbonate R-2 e was isolated in 74 % yield and 83 % ee. Furthermore, epichlorohydrin (1 f) was converted to the respective carbonate 2 f in an excellent yield of 95 % while morpholine derivative 2 g was obtained in 73 % yield. After having established a general protocol for the conversion of monosubstituted epoxides under mild conditions, the catalyst system was applied in converting disubstituted terminal epoxides. Products 2 h and 2 i were obtained in yields of 86 and 85 %, respectively, even though elevated reaction temperature (80°C) and higher CO 2 pressure (2.5 MPa) were required. Cyclic carbonates are frequently used as protecting groups for 1,2-diols. [37] The successful preparation of morpholine derivative 2 g prompted us to evaluate the synthesis of dropropizine rac-10, which is an antitussive agent typically employed as a racemic mixture in a number of commercial cough suppressant. [38] In general, it is prepared from the epoxides 1 j under acidic conditions or by direct amination of solketal, a 1,2-hydroxy-protected derivative of glycerol, via ruthenium-catalyzed hydrogen borrowing reaction and subsequent ketal hydrolysis. [39] The intermediate epoxide rac-1 j as well as enantiomerically pure R-and S-1 j were obtained in yields up to 96 % from phenylpiperazine (9) and the respective epichlorohydrin (1 f) (Scheme 2). The subsequent conversion under the standard reaction conditions for terminal epoxides gave the respective carbonate rac-2 j in 65 % after 48 h. At 45°C full conversion was achieved, and 2 j was isolated in > 99 % yield. The subsequent cleavage of the carbonate protecting group under basic conditions gave dropropizine rac-10 in 95 % yield. Notably, the formation and subsequent cleavage of the carbonate to obtain  [a] n-Butanol was employed as a solvent. [b] Yields were determined by 1 H NMR spectroscopy using mesitylene as internal standard. [c]  dropropizine in a sequential one-pot reaction could also be achieved, leading to rac-10 in 61 % yield. We envisioned that also enantiomerically pure dropropizine should be accessible via this route. Notably, this protocol circumvents the acidic hydrolysis of the epoxide to the 1,2-diol, which might lead to racemization. The precursors R-1 j and S-1 j were readily accessible from (R)-and (S)-epichlorohydrin (R-and S-1 f) and amine 9 in excellent yields and enantioselectivities of 94 % (98 % ee) and 95 % (97 % ee), respectively. The conversion of R-1 j with CO 2 at 45°C led to carbonate R-2 j in excellent 90 % yield. However, under these conditions partial racemization was observed, and R-2 j was obtained in 24 % ee. Thus, S-2 h was converted at lower temperature (23°C), which led to a significant improvement to 54 % ee but a lower yield of 61 %. The deprotection of carbonates R-2 j and S-2 j occurred stereoselectively as expected to yield enantiomerically enriched R-10 and S-10 in 95 and 99 % yield, respectively.
As the major by-product in the manufacturing of biodiesel, glycerol is widely available. [40] Thus, the use of glycerol as the feedstock for the preparation of value-added products is an attractive goal. Moreover, the use of this biobased material can lead to a significant reduction in the carbon footprint, for example, in the synthesis of carbonates, compared to their production from fossil resources. [6a] Glycidol (11 c) and its derivatives can be obtained from glycerol. [41] The respective carbonates show unique properties and find a range of applications, for example, as synthetic building blocks, monomers, and solvents. [10b,42] Hence, we were particularly interested in the preparation of cyclic carbonates 12 a-j from epoxides 11 a-j in the presence of catalyst 8 (Figure 4). Under the standard conditions the conversion of glycidyl ethers 11 a and 11 b did not lead to full conversion, and 12 a and 12 b were isolated in 56 and 58 % yield, respectively. Hence, we adjusted the reaction time to 48 h, which led to full conversion and excellent isolated yields of 96 and 97 %. The conversion of glycidol (11 c), which is susceptible to polymerization, [43] gave glycerol carbonate 12 c in 82 %. In addition, the highly fluorinated carbonates 12 d and 12 e, which can be used as electrolytes in lithium batteries, [44] were prepared in yields of 86 and 79 % respectively. Furthermore, the unsaturated carbonates 12 f and 12 g, which are potential building blocks for homoand copolymers with cyclic carbonate units in the backbone, were isolated in distinguished yields up to 99 %. [45] Epoxide 11 h, containing a furfuryl moiety, can also be synthesized from renewables, [46] and the respective carbonate was isolated in 97 % yield. Silyl-functionalized carbonates are often used as precursors for the synthesis of non-isocyanate polyhydroxyurethane hybrid materials. [47] They also find applications in industry due to their potential utilization as electrolytes [48] and in surface modification. Thus, we converted 11 i with CO 2 in the presence of catalyst 8 and were able to obtain 12 i in 93 % under slightly modified conditions. Additionally, bisphenol diglycidyl ether (11 j) was converted into the respective carbonate 12 j in 95 % yield. This biscarbonate is a frequently used monomer for the synthesis of non-isocyanate polyurethanes (NIPUs). [49] The synthesis of internal carbonates derived from epoxides and CO 2 is rather challenging and is often marginally studied in the evaluation of the substrate scope. Considering the high efficiency of catalyst 8 in the conversion of terminal epoxides under mild conditions we were interested in its performance regarding the conversion of internal epoxides 13 ( Figure 5). Initially, the standard protocol [5 mol %, 23°C, 24 h, p(CO 2 ) = 1.0 MPa] was tested for the conversion of cyclohexene oxide  [a] n-Butanol was employed as a solvent. [b] 23°C, p(CO 2 ) = 1.0 MPa. [c] Yields were determined by 1 H NMR spectroscopy using mesitylene as the internal standard.

ChemSusChem
Full Papers doi.org/10.1002/cssc.202002267 (13 a). Under these conditions < 10 % of the desired carbonate 14 a was obtained. Hence, the reaction temperature and CO 2 pressure were increased to 80°C and 2.5 MPa, respectively. This led to significant improvement of the yield, and 14 a was obtained in 59 %. Moreover, the conversion of epoxides 13 b and 13 c led to the corresponding cyclic carbonates 14 b and 14 c in 72 and 82 % yield, respectively. Notably, the conversion of cis-stilbene oxide (13 d) gave the trans-stilbene carbonate trans-14 d in a selectivity of 99 %. This indicates that the reaction proceeds via a cationic intermediate (S N 1-pathway), which is stabilized by the phenyl substituent. [34] This pathway leads to the thermodynamically more stable trans-product. Moreover, 1,2-diphenyl-ethan-1-one was observed as a byproduct, which comes from the Meinwald rearrangement. [36] In contrast, the conversion of cis-13 e and cis-methyl oleate (13 f) gave the respective carbonates in yields up to 84 % with a cis/ trans-selectivity of 25 : 75. This can be attributed to the less pronounced stabilization of the cationic intermediate by hyperconjugation in the S N 1-pathway.

DFT calculations
On the basis of our findings and previous reports [50] we propose a three-step mechanism. The initial step is the ring-opening of epoxide 1 a. Subsequently, the positively charged carbon atom of CO 2 couples with the negatively charged oxygen atom to form a linear carbonate; alternatively, this step can also be considered as a nucleophilic attack of the negatively charged oxygen atom to the lowest unoccupied molecular orbital (LUMO) of CO 2 . Finally, an intramolecular nucleophilic substitution leads to the formation of the desired cyclic carbonate and liberates the catalyst. Since the nucleophilic counterion has been found to have an important effect on the activity of the catalyst, both bromide salt 7 and iodide salt 8 were considered. On the basis of this proposal, we calculated the full Gibbs freeenergy surface for the cycloaddition of CO 2 to epoxide 1 a catalyzed by phenol-derived phosphonium halides 7 and 8, affording the five-membered cyclic carbonate 2 a. All computational details are given in the Supporting Information. Here we present the results for the more active catalyst 8, while those for the less active bromide salt 7 can be found in the Supporting Information. The optimized structure I shows a hydrogen bonding (2.297 Å) interaction between the phenolic OH and the I À counter ion. Notably, this interaction can also be seen in the crystal structure of catalyst 8 (Figure 6, O1AÀ H1A···I1A i : O1AÀ H1A = 0.89(5) Å, H1A···I1A i = 2.48(5) Å, O1A···I1A i = 3.365(3) Å, O1AÀ H1A···I1A i = 172(4)°, symmetry code: (i) À 1/2 + x,y,1/2À z).
For catalyst 8, two possible pathways for the ring-opening at the methylene (C β , Scheme 3, right) and methine carbon (C α , Scheme 3, left) in the epoxide function were evaluated.
The structure of the intermediates in the catalytic cycle are shown in Scheme 3 while for clarity the optimized structures of transition states TS1-α to TS3-α as well as TS1-β to TS3-β are shown separately in Figure 7. The corresponding Gibbs freeenergy profile for the opening at C α and C β is depicted in Figure 8. The initial step is the epoxide coordination to the phenol-derived phosphonium salt to form intermediate II via hydrogen bonding. The coordination is exergonic by 3 kJ mol À 1 . This energy difference indicates dynamic equilibrium in favor of II (77 %). The next step is the nucleophilic attack of I À to the carbon of the epoxide with CÀ O bond cleavage and the formation of a CÀ I bond.
Notably, the ring-opening at C β via transition state of TS1-β has an energy barrier of 68 kJ mol À 1 , which is lower than that at C α via transition state of TS1-α by 20 kJ mol À 1 . This can be attributed to the steric interaction as estimated on the basis of the distortion energy of epoxide. Namely, the geometrical strain energy ΔE strain of 1 a in TS1-β is 30.6 kJ mol À 1 lower than that in Figure 6. Molecular structure of catalyst 8 in the solid state. Displacement ellipsoids correspond to 30 % probability. Lower occupancy sites are omitted for clarity. The intermolecular hydrogen bond is shown as dashed line. [51] Scheme 3. Intermediates of the calculated catalytic cycle for ring-opening at the methylene (C β , right) and methine carbon (C α , left) at epoxide 1 a. TS1-α. The proton of the phenol group is transferred to the oxygen of iodo butanolate forming an ylide and iodo-butanol. The formation of III from II is endergonic by 15 and 9 kJ mol À 1 for 2-iodobutan-1-ol (III-α) and 1-iodobutan-2-ol (III-β), respectively. The co-adsorption of CO 2 from III-α and III-β to form IV-α and IV-β is also endergonic by 14 and 26 kJ mol À 1 , respectively. The energy barrier of CÀ O coupling via transition state of TS2-α and TS2-β is 40 and 57 kJ mol À 1 from III-α and III-β, respectively. The formation of 2-iodobutyl carbonate anion V-α and 1iodobutan-2-yl carbonate anion V-β in which O b is interacting with the OH of phenol is endergonic by 2 and 9 kJ mol À 1 from III-α and III-β, respectively.
For the last step (the ring-closure reaction), three possible pathways were calculated considering that three oxygen (O a / O b /O c ) in carbonate may interact with the OH group of phenol ( Figure 9). For the α route, the interaction in V-α between 2iodobutyl carbonate through O a and O c with OH of phenol is less favorable than that through O b by 21 and 8 kJ mol À 1 , respectively. This indicates the strong stabilization of the carboxylate anion through the hydrogen bonding between the OH-group of the phenol and O b and O c of the carboxylate moiety, respectively.
For the last step through the α route, the ring closure through the O a , O b , and O c routes from the most stable V-α (O b ) via TS3-α to the carbonate-catalyst adduct VI has an energy barrier of 91, 63, and 68 kJ mol À 1 , respectively. Notably, the formation of adduct VI is exergonic by 60 kJ mol À 1 . For the β route, the interaction in V-β between 2-iodobutyl carbonate through O b and O c with OH of phenol is more favorable than that through O a by 22 and 14 kJ mol À 1 , respectively. The ring closure through the O a , O b , and O c route from V-β (O b ) via TS3-β to form the adduct VI has an energy barrier of 78, 54, and 58 kJ mol À 1 , respectively. The formation of cyclic carbonate from V-β (O b ) is exergonic by 61 kJ mol À 1 . Notably, the release of the cyclic carbonate 2 a from the catalyst-carbonate adduct VI is exergonic by 14 kJ mol À 1 . This confirms the experimental finding that in the presence of catalyst 8 no product inhibition takes place. Overall, the Gibbs free-energy profile shows that intermediate II is the resting state of the catalytic cycle. Interestingly, the ring-opening and ring-closing steps have very similar effective Gibbs energy barriers of 71 and 72 kJ mol À 1 , respectively, indicating that both steps can be rate-determining.
For catalyst 7, the Gibbs free-energy profile ( Figure S22) shows that the interaction of epoxide with phenol-derived phosphonium to form intermediate II Br through the H-bond is   endergonic by 27 kJ mol À 1 . The large energy difference indicates dynamic equilibrium in favor of I Br and 1 a (> 99.99 %) rather than II Br . For the ring-opening step, the β route is also more favorable than the α route. The energy barrier of ring-opening via TS1-β Br is 97 kJ mol À 1 , which is 5 kJ mol À 1 lower than that via TS1-α Br . It is worth noting that the formation of III-β Br is highly exergonic by 22 kJ mol À 1 , while the formation of III-β I is slightly endergonic by 6 kJ mol À 1 . This indicates that the reaction with both the Br À catalyst 7 and the I À catalyst 8 can compensate the increase of energy caused by ring-opening, and the formation of 1-bromobutan-2-ol is more thermodynamically preferred. The following CÀ O coupling via TS2-β Br has an energy barrier of 51 kJ mol À 1 . For the last step of ring-closing, the effective energy barrier via TS3-β Br (O b ) from III-β Br is 86 kJ mol À 1 . In contrast to catalyst 8, the rate-determining step for the reaction in the presence of catalyst 7 is clearly the ringopening. The effective barrier regarding this step for the bromide salt 7 is 97 kJ mol À 1 , which is higher than that for iodide salt 8 (72 kJ mol À 1 ) by 25 kJ mol À 1 . This can reasonably explain the superior catalytic activity of 8 compared to catalyst 7.

Conclusions
Bifunctional phenolic phosphonium salt catalysts showed superior efficiency in converting epoxides and CO 2 into valueadded cyclic carbonates under mild and solvent-free conditions. The phenol-based phosphonium iodide 8 proved to be the most active catalyst. Notably, this catalyst showed high activity even at room temperature. Kinetic investigations revealed that the superior activity in comparison with the previously reported aliphatic catalyst 3 originates from a higher intrinsic activity as well as the absence of any product inhibition. In the model reaction the equilibrium constant K inh of the product inhibition with the aliphatic catalyst was calculated as 0.260 L mol À 1 . Moreover, the observable rate constants k obs were determined as 0.197 h À 1 (8) > 0.0605 h À 1 (3), reflecting the catalytic activity. An apparent activation energy with a value of E a = 39.6 kJ mol À 1 was estimated for the benchmark reaction with catalyst 8. The substrate scope was evaluated, and 20 terminal and 6 demanding internal epoxides were converted. Excellent results were achieved at room temperature for terminal epoxides while the conversion of internal epoxides required elevated reaction temperatures. Notably, catalyst 8 showed high functional group tolerance, and the desired cyclic carbonates were isolated in yields up to 99 % even on multi-gram scale (up to 50 g substrate). Furthermore, this method was applied in the threestep synthesis of antitussive agent dropropizine starting from epichlorohydrin and phenylpiperazine. On the basis of the experimental findings the full Gibbs free-energy surfaces for the use of phenol-derived phosphonium halides 7 and 8 as catalysts in the model reaction were calculated. The calculation confirmed the activation of the epoxide via hydrogen bonding for the iodide salt, which facilitates the ring-opening step. Notably, the effective barrier regarding this step is 97 kJ mol À 1 for the bromide and 72 kJ mol À 1 for the iodide salt, which clearly explains the difference in activity. The DFT calculations also confirmed the experimental finding that no product inhibition occurs in the presence of the phenol-based phosphonium iodide. Interestingly, for catalyst 8 the ring-opening and ringclosing steps have similar effective Gibbs energy barriers of 71 and 72 kJ mol À 1 , respectively, indicating that both steps can be rate-determining. In contrast, for catalyst 7 the rate-determining step is the epoxide opening with an effective Gibbs energy barrier of 97 kJ mol À 1 .