C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
about
Creating molecular macrocycles for anion recognitionAnion-induced dimerization of 5-fold symmetric cyanostars in 3D crystalline solids and 2D self-assembled crystals.Crystal structure of μ-cyanido-1:2κ(2) N:C-dicyanido-1κC,2κC-bis-(quinolin-8-amine-1κ(2) N,N')-2-silver(I)-1-silver(II): rare occurrence of a mixed-valence Ag(I,II) compound.
P2860
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
description
im September 2014 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована у вересні 2014
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name
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
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C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
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type
label
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
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C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
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prefLabel
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
@en
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
@nl
P2093
P356
P1476
C vs N: which end of the cyanide anion is a better hydrogen bond acceptor?
@en
P2093
Amar H Flood
Krishnan Raghavachari
Raghunath O Ramabhadran
P304
P356
10.1021/JP412816W
P407
P577
2014-09-04T00:00:00Z