Abstract
The rearrangements for 2-phospha-4-silabicyclo[1.1.0]butane, analogous to the valence isomerization of the hydrocarbons bicyclobutane, 1,3-butadiene, and cyclobutene, were studied at the (U)QCISD(T)/6-311+G**//(U)QCISD/6-31G* level of theory. The monocyclic 1,2-dihydro-1,2-phosphasiletes are shown to be the thermodynamically preferred product, in contrast to the isomerization of the hydrocarbons, which favors the 1,3-butadiene structure. Furthermore, an unprecedented direct isomerization pathway to the 1,2-dihydro-1,2-phosphasiletes was identified. This pathway is competitive with the isomerization via the open-chain butadienes and becomes favorable when electron-donating substituents are present on silicon.
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Introduction
Bicyclo[1.1.0]butane with its strain energy of over 60 kcal mol−1 is a fascinating compound that has attracted the interest of both experimental and theoretical chemists [1]. It is now well established that bicyclo[1.1.0]butane (1) opens to the more stable valence isomer gauche-butadiene (2) by a pericyclic rearrangement, which is characterized by a concerted, asynchronous conrotatory ring opening where the central C–C bond remains intact [2, 3]. This is an allowed [σ2s+σ2a] conrotatory rearrangement according to the Woodward–Hoffmann (W–H) orbital-symmetry rules [4–6], affording kinetic intermediate 2 that can easily rotate to s-trans-1,3-butadiene (3). The activation barrier of 41.5 kcal mol−1 calculated at the multiconfiguration self-consistent field level of theory [2] agrees closely with the experimental value of 40.6 kcal mol−1 [7, 8]. The disrotatory, W–H forbidden, thermal ring opening of 1 is less favorable, and was calculated to be about 15 kcal mol−1 higher in energy [2]. Another rearrangement is also feasible; stretching of the central C–C bond leads to a planar singlet diradical transition structure for inversion, which is also a higher energy process with a barrier of 47.4 kcal mol−1 [9].
Valence isomer cyclobutene (4) is of intermediate stability between 1 and 3 and converts thermally to gauche-butadiene 2 by an electrocyclic ring opening [10, 11]. This pericyclic rearrangement follows a W–H allowed concerted, conrotatory pathway. The calculated activation barrier at the MP2/6-311G** level of theory of 33.7 kcal mol−1 [12–14] for this process is in agreement with the experimental value of 32.9±0.5 kcal mol−1 [10, 11]. Usually for the ring opening of cyclobutenes, steric effects dominate the preference for inward versus outward rotation [15]. However, electronic effects can also dictate this rearrangement, as was reported very recently for the sterically hindered substrate 5, which prefers to react via the more crowded inward rotatory pathway, leading mainly to butadiene 6 (Scheme 1) [16, 17].
Bicyclo[1.1.0]butanes with main-group hetero-elements in the ring have also received considerable attention [18]. However, little is known about the phosphorus-containing analogues [19–22]. In our ongoing research on small strained organophosphorus ring systems, we became interested in the yet unknown 2-phospha-4-silabicyclo[1.1.0]butanes, whose occurrence we reported as a reactive intermediate recently [23, 24]. Valence isomerization of the 2-phospha-4-silabicyclo[1.1.0]butane 9 to the 1,2-dihydro-1,2-phosphasiletes 10a,b was indicated by reacting 1H-phosphirene 8 with silylene Si[(NCH t2 Bu)2C6H4-1,2] [≡Si(NN)] (Scheme 2).
SCS-MP2/6-311+G** calculations on B3LYP/6-31G* model structures show that the intermediate 2-phospha-4-silabicyclo[1.1.0]butane isomerizes directly, via an unprecedented W–H allowed [σ2s+σ2a] process, to the thermodynamically preferred 1,2-dihydro-1,2-phosphasilete [23, 24]. This pathway is favored over the concerted, asynchronous conrotatory ring opening leading to s-trans-1-phospha-4-sila-1,3-butadiene [25].
Here, we report on the isomerization of 2-phospha-4-silabicyclo[1.1.0]butane A to its valence isomers 1-phospha-4-sila-1,3-butadiene B and 1,2-dihydro-1,2-phosphasilete C (only one other synthesis of 1,2-dihydro-1,2-phosphasiletes was reported: [26–28]), using high-level ab initio calculations at the (U)QCISD(T)/6-311+G**//(U)QCISD/6-31G* level of theory. We will compare the differences between a direct A→C pathway versus the isomerization via butadiene B. In addition, the influence of substituents on silicon on the rearrangements will also be discussed.
Computational details
All calculations were performed using the GAUSSIAN 98 [29] suite of programs. Geometries were optimized using the standard 6-31G* basis set at the (U)MP2 and (U)QCISD [30, 31] level of theory, while single-point calculations were preformed at the (U)QCISD(T)/6-311+G** level using the (U)QCISD/6-31G* geometries. First and second order energy derivatives were computed to confirm that minima or transition structures had been located at the (U)MP2/6-31G* level. Intrinsic reaction coordinate driving calculations were performed at the (U)MP2/6-31G* level to establish the connections between transition structures and minima. The total energies calculated at the (U)MP2, (U)QCISD, and (U)QCISD(T) levels were corrected for the (U)MP2/6-31G* level zero-point energies scaled by a factor of 0.967 [32].
Results and discussion
First, we investigated the rearrangements of bicyclo[1.1.0]butane (1) and cyclobutene (4) into the more stable s-trans-1,3-butadiene (3) at the (U)QCISD(T)/6-311+G**//(U)QCISD/6-31G* level of theory (this method gives similar energies when compared to the CASSCF(10,10)/6-31G* level of theory as was reported for the isomerization of 2-oxabicyclo[1.1.0]butane: [33]), since no complete study of the valence isomerizations of all C4H6 isomers at the same level of theory were reported to date. Subsequently, we investigated the rearrangements of the 2-phospha-4-silabicyclo[1.1.0]butanes, where the effects of heteroatom substitution on the characteristics of the rearrangements become apparent.
Bicyclo[1.1.0]butane (1) leads to gauche-butadiene 2 via a concerted, asynchronous conrotatory ring opening [2, 3], which has a barrier of 39.2 kcal mol−1, and is exothermic by 26.0 kcal mol−1 (Fig. 1). This closed-shell rearrangement is favored over the corresponding diradical open-shell pathway (ΔE ‡=43.2 kcal mol−1, <S 2>=0.85). In addition, cyclobutene (4) also gives 2 via a synchronous (Cs symmetry) conrotatory ring opening [12–14] that requires 32.8 kcal mol−1, and is exothermic by 9.9 kcal mol−1. Both calculated reaction barriers are in excellent agreement with the experimental values of 40.6 kcal mol−1 [7, 8] and 32.9 kcal mol−1 [10, 11], respectively.
The kinetic gauche-butadiene 2 can easily transform into its enantiomer 2′ via the planar s-cis-1,3-butadiene (TS2-2′) [2, 34] with a barrier of only 0.7 kcal mol−1, or can rotate to the more stable trans-butadiene 3 (ΔE ‡=2.5 kcal mol−1) with an exothermicity of 2.6 kcal mol−1 (Fig. 2) [12–14]. The geometrical parameters of the optimized structures 1, 3, and 4 at the QCISD/6-31G* level of theory are in excellent agreement with the experimental estimates (experimental structures—1, 3, and 4: [35–37]).
Incorporating heteroatoms into the bicyclo[1.1.0]butane framework has a profound impact. We found that 2-phospha-4-silabicyclo[1.1.0]butane (11) opens with a modest exothermicity (0.4 kcal mol−1) directly to valence isomer s-1-phospha-4-sila-1,3-butadiene (12) in its trans configuration via a concerted, asynchronous conrotatory ring opening. In this process, the P–C2 bond becomes elongated well before that of the Si–C1 bond (Fig. 3).
The activation barrier of 38.8 kcal mol−1 is very similar to the calculated activation barrier of 39.2 kcal mol−1 for the [σ2s+σ2a] process in bicyclo[1.1.0]butane (1). The closed-shell rearrangement 11→12 is favored over the corresponding diradical open-shell pathway (ΔE ‡=41.3 kcal mol−1, <S 2>=0.97).
s-Trans-butadiene 12 can transform into the slightly less stable gauche-butadiene 13 (ΔE=2.6 kcal mol−1) with an energy barrier of 7.5 kcal mol−1. Subsequently, butadiene 13 can isomerize via a conrotatory electrocyclic ring closure to the much more stable 1,2-dihydro-1,2-phosphasilete (14) (ΔE=−23.9 kcal mol−1), with a rearrangement barrier of only 3.2 kcal mol−1. Clearly, if a 1-phospha-4-sila-butadiene is to be formed from 11, it will rearrange to the four-membered ring structure 14. We conclude that in contrast to the hydrocarbons, where butadiene 3 is the favored product, the P,Si-derivatives 12 and 13 are not likely candidates to be observed on rearranging bicyclic compound 11.
As 14 is thermodynamically the preferred valence isomer, we also explored whether it could be formed directly from bicyclic 11. Indeed, forcing an asynchronous conrotatory ring opening with an initial SiH2-group rotation resulted in a transition structure TS11–14 for the direct rearrangement of 11 into 14 (Fig. 4). The barrier of 39.0 kcal mol−1 for this closed-shell process is similar to the conversion via the P,Si-butadienes (ΔE ‡=38.8 kcal mol−1, Fig. 3)Footnote 1. The rearrangement via TS11–14 obeys the orbital symmetry rules and can be described as a [σ2s+σ2a] process. Such a pathway is unprecedented for the isomerization of the carbon analogue bicyclo[1.1.0]butane (1) [2], for which s-trans-1,3-butadiene is the favored product.
Due to the similarities in activation energy for the conversions 11→12 and 11→14 at the QCISD(T)/6-311+G**//QCISD/6-31G* level of theory, we have also incorporated in our computational model the cyclic diamine HN-C=C-NH as substituent on silicon to investigate the effect of donating N atoms, which are also present in our experimental system [23, 24] on the rearrangements.
Substituted 2-phospha-4-silabicyclo[1.1.0]butane 15 leads to its valence isomer s-trans-1-phospha-4-sila-1,3-butadiene 16 via a concerted, asynchronous conrotatory ring opening (ΔE ‡=39.0 kcal mol−1), with a modest endothermicity of 1.5 kcal mol−1 (Fig. 5). The associated transition structure TS15–16 shows features similar to the parent analogue TS11–12, and the closed-shell rearrangement 15→16 is favored over the corresponding diradical open-shell pathway (ΔE ‡=46.1 kcal mol−1, <S 2>=0.97)Footnote 2. In addition, s-trans-butadiene 16 can transform into the slightly more stable planar cis-butadiene 17 (ΔE=−1.5 kcal mol−1), which is now an energy minimum, with an energy barrier of only 8.2 kcal mol−1.
Subsequently, 17 can isomerize via a conrotatory electrocyclic ring closure to the much more stable 1,2-dihydro-1,2-phosphasilete 18 (ΔE=−25.6 kcal mol−1) with a minute barrier of only 1.3 kcal mol−1. The geometrical parameters of the optimized 18 are in good agreement with the single-crystal X-ray analysis of 10a [23, 24].
Interestingly, the direct valence isomerization now becomes favorable, and 2-phospha-4-silabicyclo[1.1.0]butane 15 gives cyclobutene derivative 18 (ΔE ‡=27.7 kcal mol−1) via a W–H allowed [σ2s+σ2a] process, with an exothermicity of 25.6 kcal mol−1 (Fig. 6).
The lower barrier for the direct conversion 15→18 compared to that of the parent 11→14 can be ascribed to the presence of the donating amino groups on silicon. Generally, π-donor (e.g., NH2) and σ-acceptor (e.g., F) substituents destabilize three-membered rings, making them more reactive, as indicated by their increased ring strain [38, 39]. This is also evident for the 15→18 conversion by an increased exothermicity (ΔE 11→14 =21.7 kcal mol−1; ΔE 15→18 =25.6 kcal mol−1). Additionally, the analogous rearrangement for the fluoro-substituted 2-phospha-4-silabicyclo[1.1.0]butane 19 confirms this trend (ΔE 19→20 =28.1 kcal mol−1, Fig. 7). Furthermore, the associated transition state of this novel pathway is stabilized by the electron-donating N-heterocyclic substituent on silicon (ΔE ‡ 11→14 =39.0 kcal mol−1; ΔE ‡ 15→18 =27.7 kcal mol−1; ΔE ‡ 19→20 =35.0 kcal mol−1).
Conclusions
Hetero substitution changes the stability of the valence isomers of bicyclo[1.1.0]butane (1). 2-Phospha-4-silabicyclo[1.1.0]butane (11) is the least stable isomer and 1,2-dihydro-1,2-phosphasilete (14) the most stable one at the QCISD(T)/6-311+G**//QCISD/6-31G* level of theory [40]. Two reaction pathways for the thermal isomerization of 2-phospha-4-silabicyclo[1.1.0]butane (11) have been found: (a) a three-step process starting with a barrier of 38.8 kcal mol−1 for the concerted, asynchronous conrotatory ring opening of 11 to s-trans-1-phospha-4-sila-1,3-butadiene (12), followed by a conformational change to the gauche isomer 13 and a subsequent conrotatory electrocyclic ring closure to 14, and (b) a direct transformation of 11 into 14 via a [σ2s+σ2a] process with a barrier of 39.0 kcal mol−1 which becomes favorable when electron-donating substituents are present on silicon. This latter path is unprecedented for the analogous isomerization of bicyclo[1.1.0]butane.
Cartesian coordinates and energies of all stationary points are available in the electronic supplementary material.
Notes
No competitive open-shell rearrangement is present for TS11–14.
Open-shell TS15–16 was calculated at the UQCISD(T)/6-311+G**//UMP2/6-31G* level of theory.
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Dedicated to Professor Dr. Paul von Ragué Schleyer on the occasion of his 75th birthday.
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Slootweg, J.C., Ehlers, A.W. & Lammertsma, K. Valence isomerization of 2-phospha-4-silabicyclo[1.1.0]butane: a high-level ab initio study. J Mol Model 12, 531–536 (2006). https://doi.org/10.1007/s00894-005-0041-7
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DOI: https://doi.org/10.1007/s00894-005-0041-7