Halogen bonding in 5-iodo-1-arylpyrazoles investigated in the solid state and predicted by solution13C-NMR spectroscopy-Reference-Cited by-同舟云学术

Halogen bonding in 5-iodo-1-arylpyrazoles investigated in the solid state and predicted by solution13C-NMR spectroscopy

Published:2019 Issue:46 Volume:21 Page:7085-7093
ISSN:1466-8033
Container-title:CrystEngComm
language:en
Short-container-title:CrystEngComm

Author:

Popa Marcel Mirel¹²³⁴^ORCID,Man Isabela Costinela¹²³⁴,Draghici Constantin¹²³⁴,Shova Sergiu⁵⁶²⁴,Caira Mino R.⁷⁸⁹¹⁰^ORCID,Dumitrascu Florea¹²³⁴^ORCID,Dumitrescu Denisa¹¹¹²⁴

Affiliation:

1. “C.D. Nenitzescu” Center for Organic Chemistry

2. Romanian Academy

3. Bucharest

4. Romania

5. “Petru Poni” Institute of Macromolecular Chemistry

6. Department of Inorganic Polymers

7. Department of Chemistry

8. University of Cape Town

9. Rondebosch 7701

10. South Africa

11. Ovidius University Constanta

12. Faculty of Pharmacy

Abstract

Halogen bonding as important directional forces in the supramolecular structure of iodinated 1-arylpyrazoles.

Publisher

Royal Society of Chemistry (RSC)

Subject

Condensed Matter Physics,General Materials Science,General Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/CE/C9CE01263J

Reference76 articles.

1. The Halogen Bond

2. Definition of the halogen bond (IUPAC Recommendations 2013)

3. Halogen Bonds in Crystal Engineering: Like Hydrogen Bonds yet Different

4. Type II halogen···halogen contacts are halogen bonds

5. Hydrogen and halogen bonds are ruled by the same mechanisms

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