An Investigation of the Hydrogen-Bond Preferences and Co-crystallization Behavior of Three Didonor Compounds.-Reference-Cited by-同舟云学术

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An Investigation of the Hydrogen-Bond Preferences and Co-crystallization Behavior of Three Didonor Compounds.

Published:2011-04-11 Issue:5 Volume:11 Page:2011-2019
ISSN:1528-7483
Container-title:Crystal Growth & Design
language:en
Short-container-title:Crystal Growth & Design

Author:

Lemmerer Andreas¹,Adsmond Daniel A.²,Bernstein Joel³

Affiliation:

1. Molecular Sciences Institute, School of Chemistry, University of the Witwatersrand, Johannesburg 2050, South Africa.

2. Ferris State University, Department of Physical Sciences, Big Rapids, Michigan, 49307, USA.

3. Department of Chemistry, Ben-Gurion University of the Negev, Beer Sheva, Israel, 84105.

Publisher

American Chemical Society (ACS)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/cg2002145

Reference41 articles.

1. Crystal Engineering Using Multiple Hydrogen Bonds

2. Molecular Recognition in the Solid State: Hydrogen-Bonding Control of Molecular Aggregation

3. Designer crystals: intermolecular interactions, network structures and supramolecular synthons

4. The probable number of hydrogen-bonded contacts for chemical groups in organic crystal structuresElectronic supplementary information (ESI) available: details of the calculated properties of atoms and groups in Tables 1 and 2. See http://www.rsc.org/suppdata/cc/b4/b402939a/

5. “STRONG” HYDROGEN BONDS IN CHEMISTRY AND BIOLOGY

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3. 3. Qualitative and quantitative crystal engineering of multi-functional co-crystals;Multi-Component Crystals;2017-11-20

4. Design and Synthesis of Ternary Cocrystals Using Carboxyphenols and Two Complementary Acceptor Compounds;Crystal Growth & Design;2015-12-10

5. Influence of the halogen substituent on the formation of halogen and hydrogen bonding in co-crystals formed from acridine and benzoic acids;CrystEngComm;2015

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