A Cambridge Structural Database analysis of the C–H⋯Cl interaction: C–H⋯Cl− and C–H⋯Cl–M often behave as hydrogen bonds but C–H⋯Cl–C is generally a van der Waals interaction-Reference-Cited by-同舟云学术

A Cambridge Structural Database analysis of the C–H⋯Cl interaction: C–H⋯Cl− and C–H⋯Cl–M often behave as hydrogen bonds but C–H⋯Cl–C is generally a van der Waals interaction

Published:2001 Issue:27 Volume:3 Page:114-119
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Thallapally Praveen K.,Nangia Ashwini

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2001/CE/B102780H

Reference24 articles.

1. Metal-bound chlorine often accepts hydrogen bonds

2. Fluoride ligands exhibit marked departures from the hydrogen bond acceptor behavior of their heavier halogen congeners

3. Hydrogen-Bond Distances to Halide Ions in Organic and Organometallic Crystal Structures: Up-to-date Database Study

4. A statistical analysis of halide · · · H–A (A = OR, NR2, N+R3) hydrogen bonding interactions in the solid state

5. Bis(diphenylphosphino)methane and related ligands as hydrogen bond donors†

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