Elemination Reactions of α-Halogenated Ketones. XII.1aCarbon-Halogen and Carbon-Hydrogen Bond Strengths as Orientation and Rate-Determining Factors. Deuterium Isotope Effects in Dehydrobromination of 2-Bromo-2-benzyl-1-indanone1b

1964 ◽  
Vol 86 (8) ◽  
pp. 1553-1557 ◽  
Author(s):  
Dennis N. Kevill ◽  
Guillaume A. Coppens ◽  
Norman H. Cromwell
1982 ◽  
Vol 35 (7) ◽  
pp. 1281 ◽  
Author(s):  
JR Khurma ◽  
DV Fenby

Liquid-liquid phase diagrams have been measured for the systems CH3OH+n-C6H14, CH3OH + n-C6D14, CH3OD + n-C6HI4 and CH3OD + n-C6D14. The upper critical solution temperatures of these systems are 306.70, 304.30, 307.59 and 304.84 K, respectively. The results are in accord with the qualitative predictions of the Rabinovich theory, which considers hydrogen bond and London dispersion interactions.


Molecules ◽  
2021 ◽  
Vol 26 (9) ◽  
pp. 2409
Author(s):  
Poul Erik Hansen

Intramolecular NH…O,S,N interactions in non-tautomeric systems are reviewed in a broad range of compounds covering a variety of NH donors and hydrogen bond acceptors. 1H chemical shifts of NH donors are good tools to study intramolecular hydrogen bonding. However in some cases they have to be corrected for ring current effects. Deuterium isotope effects on 13C and 15N chemical shifts and primary isotope effects are usually used to judge the strength of hydrogen bonds. Primary isotope effects are investigated in a new range of magnitudes. Isotope ratios of NH stretching frequencies, νNH/ND, are revisited. Hydrogen bond energies are reviewed and two-bond deuterium isotope effects on 13C chemical shifts are investigated as a possible means of estimating hydrogen bond energies.


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