The platform will undergo maintenance on Sep 14 at about 7:45 AM EST and will be unavailable for approximately 2 hours.
2022
DOI: 10.3390/cryst12020133
|View full text |Cite
|
Sign up to set email alerts
|

Editorial: Advanced Research in Halogen Bonding

Abstract: The Special Issue on “Advanced Research in Halogen Bonding” is a collection of 17 original articles reporting the results of theoretical and experimental studies that provide new insights into this fascinating intermolecular interaction [...]

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
1
0

Year Published

2022
2022
2022
2022

Publication Types

Select...
1

Relationship

0
1

Authors

Journals

citations
Cited by 1 publication
(1 citation statement)
references
References 17 publications
(17 reference statements)
0
1
0
Order By: Relevance
“…Carbon-bound halogen atoms have nucleophilic and electrophilic parts; (a) the electrophilic part is due to the electron deficiency along the C-X bond, and hence there is a formation of a positive electrostatic potential end cap, which is known as s-hole. [1][2][3][4][5][6][7][8] The interaction of the electrophilic part of the covalently bonded halogen atom with nucleophiles is known as a halogen bond (D-XÁ Á ÁA), where D-X is the halogen bond donor and A is the halogen bond acceptor. The XÁ Á ÁA distance is usually less than the sum of van der Waals radii of X and A, and the D-XÁ Á ÁA angle is essentially linear.…”
Section: Introductionmentioning
confidence: 99%
“…Carbon-bound halogen atoms have nucleophilic and electrophilic parts; (a) the electrophilic part is due to the electron deficiency along the C-X bond, and hence there is a formation of a positive electrostatic potential end cap, which is known as s-hole. [1][2][3][4][5][6][7][8] The interaction of the electrophilic part of the covalently bonded halogen atom with nucleophiles is known as a halogen bond (D-XÁ Á ÁA), where D-X is the halogen bond donor and A is the halogen bond acceptor. The XÁ Á ÁA distance is usually less than the sum of van der Waals radii of X and A, and the D-XÁ Á ÁA angle is essentially linear.…”
Section: Introductionmentioning
confidence: 99%