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- W2056329517 abstract "The unimolecular decomposition of substituted acetamidines XC(NH)NH2, where X = CH3(I), CH2F (II), CHF2(III), CF3(IV), CH2NH2(V) and CH2NO2(VI) has been examined by ab initio methods using the 4-31G standard basis set. The process has an asynchronous mechanism. Transition structures for all the compounds can be described as four-membered rings. The influence of sub-stitution on the decomposition process is discussed in terms of a modified version of a More O'Ferrall–Jencks type diagram. The effects of functional groups are larger in a perpendicular than a parallel orientation to the reaction path; this is an example of the ‘anti-Hammond’ effect." @default.
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- W2056329517 date "1991-01-01" @default.
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- W2056329517 title "Theoretical studies of substituent effects on stationary structures of amidine decomposition" @default.
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