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HK Oh

Publications and source records attributed to HK Oh.

3 recordsLinked to original sources
PubMed2000

Kinetics and mechanism of addition of benzylamines to benzylidene-1,3-indandiones in acetonitrile

Nucleophilic addition reactions of benzylamines (BA; XC6H4CH2NH2) to benzylidene-1,3-indandiones (BID; YC6H4CH=C(C=O)2C6H4) have been studied in acetonitrile at 25.0 degrees C. The rate is first-order with respect to BA and BID, and no base catalysis is observed. The structure-reactivity behaviors (k2, rhoX, betaX, and betaY) are intermediate between the two series of addition reactions of BA to beta-nitrostyrene (NS) and benzylidenemalononitrile (BMN) in acetonitrile. The normal kinetic isotope effects, kH/kD > 1.0, involving deuterated BAs (XC6H4CH2ND2) are smaller than those for the reactions of NS and BMN suggesting a somewhat looser bond formation in the transition state. The reaction is predicted to proceed in a single step with concurrent C(alpha)-N bond formation and proton transfer to C(beta). A hydrogen-bonded, four-center type cyclic transition state is proposed.

Journal Article↗
PubMed2000

Kinetics and mechanism of the addition of benzylamines to benzylidenemalononitriles in acetonitrile

Nucleophilic addition reactions of benzylamines (BA) to benzylidenemalononitrile (BMN) have been studied in acetonitrile at 15.0 degrees C. The rate is first-order with respect to both BA and BMN and no base catalysis is observed. The rate decreases as the electron-withdrawing power of the substituent (Y) in the substrate increases (rho Y < 0). This is in contrast to the similar reactions of beta-nitrostyrenes (NS) with BAs in acetonitrile and the addition reactions of NS and BMN in aqueous solution (rho Y > 0). This sign change of rho Y is considered to result from the strong electron-withdrawing power of the (CN)2 group in BMN, which leads to polarization of C alpha delta+C delta- (CN)2 in the transition state. The mechanism of amine addition to BMN in acetonitrile is radically different from that in water. The reaction is predicted to proceed concertedly in a single step with a hydrogen-bonded, four-center cyclic transition state.

Journal Article↗