Literature DB >> 26886515

σ-Hole Bond vs π-Hole Bond: A Comparison Based on Halogen Bond.

Hui Wang1, Weizhou Wang2, Wei Jun Jin1.   

Abstract

The σ-hole and π-hole are the regions with positive surface electrostatic potential on the molecule entity; the former specifically refers to the positive region of a molecular entity along extension of the Y-Ge/P/Se/X covalent σ-bond (Y = electron-rich group; Ge/P/Se/X = Groups IV-VII), while the latter refers to the positive region in the direction perpendicular to the σ-framework of the molecular entity. The directional noncovalent interactions between the σ-hole or π-hole and the negative or electron-rich sites are named σ-hole bond or π-hole bond, respectively. The contributions from electrostatic, charge transfer, and other terms or Coulombic interaction to the σ-hole bond and π-hole bond were reviewed first followed by a brief discussion on the interplay between the σ-hole bond and the π-hole bond as well as application of the two types of noncovalent interactions in the field of anion recognition. It is expected that this review could stimulate further development of the σ-hole bond and π-hole bond in theoretical exploration and practical application in the future.

Entities:  

Year:  2016        PMID: 26886515     DOI: 10.1021/acs.chemrev.5b00527

Source DB:  PubMed          Journal:  Chem Rev        ISSN: 0009-2665            Impact factor:   60.622


  36 in total

1.  On the ability of pnicogen atoms to engage in both σ and π-hole complexes. Heterodimers of ZF2C6H5 (Z = P, As, Sb, Bi) and NH3.

Authors:  Wiktor Zierkiewicz; Mariusz Michalczyk; Rafał Wysokiński; Steve Scheiner
Journal:  J Mol Model       Date:  2019-05-08       Impact factor: 1.810

2.  Theoretical study of noncovalent interactions in XCN···YO2H (X = F, Cl, Br, I; Y = P, As, Sb) complexes.

Authors:  Qiang Zhao
Journal:  J Mol Model       Date:  2017-05-12       Impact factor: 1.810

3.  A theoretical investigation on the complexes of B3O3H3 with acetylene and its substituted derivatives.

Authors:  Lijuan Zhang; Dazhi Li
Journal:  J Mol Model       Date:  2019-11-07       Impact factor: 1.810

4.  Halogen-π Interactions in the Cytochrome P450 Active Site: Structural Insights into Human CYP2B6 Substrate Selectivity.

Authors:  Manish B Shah; Jingbao Liu; Qinghai Zhang; C David Stout; James R Halpert
Journal:  ACS Chem Biol       Date:  2017-04-06       Impact factor: 5.100

5.  A density functional theory study on the interactions between dibenzothiophene and tetrafluoroborate-based ionic liquids.

Authors:  Jin Lin; Renqing Lü; Chongchong Wu; Ye Xiao; Fei Liang; Temilola Famakinwa
Journal:  J Mol Model       Date:  2017-03-31       Impact factor: 1.810

Review 6.  The Pnictogen Bond: The Covalently Bound Arsenic Atom in Molecular Entities in Crystals as a Pnictogen Bond Donor.

Authors:  Arpita Varadwaj; Pradeep R Varadwaj; Helder M Marques; Koichi Yamashita
Journal:  Molecules       Date:  2022-05-25       Impact factor: 4.927

Review 7.  The Relevance of Experimental Charge Density Analysis in Unraveling Noncovalent Interactions in Molecular Crystals.

Authors:  Sajesh P Thomas; Amol G Dikundwar; Sounak Sarkar; Mysore S Pavan; Rumpa Pal; Venkatesha R Hathwar; Tayur N Guru Row
Journal:  Molecules       Date:  2022-06-08       Impact factor: 4.927

8.  Mechanism and Origins of Chemo- and Stereoselectivities of Aryl Iodide-Catalyzed Asymmetric Difluorinations of β-Substituted Styrenes.

Authors:  Biying Zhou; Moriana K Haj; Eric N Jacobsen; K N Houk; Xiao-Song Xue
Journal:  J Am Chem Soc       Date:  2018-11-05       Impact factor: 15.419

9.  Inorganic benzenes as the noncovalent interaction donor: a study of the π-hole interactions.

Authors:  Runtian Chu; Xueying Zhang; Lingpeng Meng; Yanli Zeng
Journal:  J Mol Model       Date:  2017-11-08       Impact factor: 1.810

10.  Theoretical study on the noncovalent interactions involving triplet diphenylcarbene.

Authors:  Chunhong Zhao; Hui Lin; Aiting Shan; Shaofu Guo; Xiaoyan Li; Xueying Zhang
Journal:  J Mol Model       Date:  2021-07-09       Impact factor: 1.810

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