α-bond stretching:: A static approach for dynamic process
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Scheschkewitz, D
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机构:Univ Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USA
Scheschkewitz, D
Amii, H
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机构:Univ Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USA
Amii, H
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Gornitzka, H
Schoeller, WW
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机构:Univ Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USA
Schoeller, WW
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Bourissou, D
Bertrand, G
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Univ Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USAUniv Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USA
Bertrand, G
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机构:
[1] Univ Calif Riverside, Dept Chem, CNRS, UMR 2282,Joint Res Chem Lab, Riverside, CA 92521 USA
[2] Univ Toulouse 3, CNRS, UMR 5069, Lab Heterochim Fondamentale & Appliquee, F-31062 Toulouse 04, France
Ring stretching: The reaction profile corresponding to the inversion of bicyclo[1.1.0] butane derivatives, including the cyclobutane-1,3-diyl transition state, has been modeled by the preparation of a series of boron-phosphorus-containing analogues (see picture: P red; B blue). These differ only in the substituents around the B2P2 core, yet a variation of 40% in the boron-boron separation is observed.