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Theoretical study of mechanism of cycloaddition reaction between dimethylmethylenesilylene and formaldehyde
Author(s) -
Lu Xiu Hui,
Yu Hai Bin,
Che Xin,
Xiang Ping Ping
Publication year - 2008
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.21608
Subject(s) - exothermic reaction , chemistry , cycloaddition , singlet state , reaction mechanism , potential energy surface , formaldehyde , transition state , energy profile , computational chemistry , activation barrier , reaction intermediate , activation energy , photochemistry , density functional theory , molecule , organic chemistry , catalysis , energy (signal processing) , excited state , atomic physics , physics , statistics , mathematics
Abstract The mechanism of cycloaddition reaction between singlet dimethylmethylenesilylene and formaldehyde has been investigated with MP2/6‐31G* method, including geometry optimization and vibrational analysis for the involved stationary points on the potential energy surface. The energies of different conformations are calculated by CCSD(T)//MP2/6‐31G* method. From the potential energy surface, it can be considered in thermodynamics and dynamics that reaction (1) and reaction (4) are the two dominant competitive reaction channels of cycloaddition reaction between dimethylmethylenesilylene and formaldehyde. The reaction process of reaction (1) is that: the two reactants (R1, R2) first form intermediates INT1a and INT1b through two reaction paths, a and b, which are barrier‐free exothermic reactions of 31.8 and 43.9 kJ/mol; then, INT1a and INT1b isomerize to a four‐membered ring product P1 via transition states TS1a and TS1b, with energy barriers of 26.3 and 24.4 kJ/mol. Reaction (4) also has two reaction paths, a and b, each of which consists of three steps are as follows: (i) the two reactants (R1, R2) first form intermediates INT3a and INT3b, which are barrier‐free exothermic reactions of 64.5 and 44.2 kJ/mol. (ii) INT3a and INT3b further react with formaldehyde (R2) to form intermediates INT4a and INT4b, through barrier‐free exothermic reactions of 22.9 and 22.2 kJ/mol. (iii) INT4a and INT4b then isomerize to form silapolycyclic product P4 via transition states TS4a and TS4b, with energy barriers of 39.7 and 29.3 kJ/mol. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2008

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