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Volumn 32, Issue 8, 2011, Pages 2628-2632

Transition state variation in the anilinolysis of O-aryl phenyl phosphonochloridothioates in acetonitrile

Author keywords

Cross interaction constant; Deuterium kinetic isotope effect; O Aryl phenyl phosphonochloridothioates; Phosphoryl transfer reaction; Transition state variation

Indexed keywords

CROSS-INTERACTION CONSTANTS; DEUTERIUM KINETIC ISOTOPE EFFECT; O-ARYL PHENYL PHOSPHONOCHLORIDOTHIOATES; PHOSPHORYL TRANSFER REACTION; TRANSITION STATE VARIATION;

EID: 80052013012     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2011.32.8.2628     Document Type: Article
Times cited : (24)

References (76)
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    • Coetzee, J. F., Ritchie C. D., Eds.; Marcel Dekker: New York Chapter 4
    • (a) Ritchie, C. D. In Solute-Solvent Interactions; Coetzee, J. F., Ritchie, C. D., Eds.; Marcel Dekker: New York, 1969; Chapter 4.
    • (1969) Solute-Solvent Interactions
    • Ritchie, C.D.1
  • 61
    • 33751499211 scopus 로고
    • Perrin and his coworkers reported that the basicities of β-deuterated analogs of benzylamine, N,N-dimethylaniline and methylamine increase roughly by 0.02 pKa units per deuterium, and that these effects are additive; (a) Perrin, C. I.; Engler, R. E. J. Phys. Chem. 1991, 95, 8431.
    • (1991) J. Phys. Chem. , vol.95 , pp. 8431
    • Perrin, C.I.1    Engler, R.E.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.