Cooperative non-covalent interactions and synthetic feed as driving forces to structural diversity within organic co-crystals containing isosteric perhalobenzenes-Reference-Cited by-同舟云学术

Cooperative non-covalent interactions and synthetic feed as driving forces to structural diversity within organic co-crystals containing isosteric perhalobenzenes

Published:2022 Issue:21 Volume:24 Page:3841-3845
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Bosch Eric¹^ORCID,Ferrence Gregory M.²^ORCID,Powell Conrad J.³^ORCID,Unruh Daniel K.⁴^ORCID,Krueger Herman R.³,Groeneman Ryan H.³^ORCID

Affiliation:

1. Department of Chemistry, Missouri State University, Springfield, MO 65897, USA

2. Department of Chemistry, Illinois State University, Normal, IL, 61790, USA

3. Department of Biological Sciences, Webster University, St. Louis, MO 63119, USA

4. Department of Chemistry and Biochemistry, Texas Tech University, Lubbock, TX, 79409, USA

Abstract

Structural diversity is achieved in a series of halogen-bonded co-crystals based upon cooperative non-covalent interactions and the synthetic feed of the components.

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/CE/D2CE00360K

Reference23 articles.

1. Cytochrome P450—The Wonderful Nanomachine Revealed through Dynamic Simulations of the Catalytic Cycle

2. Halogen bonding in the co-crystallization of potentially ditopic diiodotetrafluorobenzene: a powerful tool for constructing multicomponent supramolecular assemblies

3. Halogen and Hydrogen Bonding in Multicomponent Crystals of Tetrabromo-1H-Benzotriazole

4. Harnessing Noncovalent Interactions for a Directed Evolution of a Six-Component Molecular Crystal

5. Equivalence of Ethylene and Azo-Bridges in the Modular Design of Molecular Complexes: Role of Weak Interactions

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