Electrophilicity and Nucleophilicity of Boryl Radicals

被引:59
|
作者
Wu, Chao [1 ]
Hou, Xiufang [2 ]
Zheng, Yuheng [1 ]
Li, Pengfei [1 ]
Lu, Dongmei [3 ]
机构
[1] Xi An Jiao Tong Univ, Frontier Inst Sci & Technol, Xian 710054, Peoples R China
[2] Yanan Univ, Coll Chem & Chem Engn, Yanan 716000, Peoples R China
[3] Xi An Jiao Tong Univ, Sch Sci, Dept Appl Chem, Xian 710049, Peoples R China
来源
JOURNAL OF ORGANIC CHEMISTRY | 2017年 / 82卷 / 06期
基金
美国国家科学基金会;
关键词
LEWIS-BASES; REACTIVITY; COORDINATION; CATALYSIS; BORANES; BOND;
D O I
10.1021/acs.joc.6b02849
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
We carried out a survey of the relative reactivity of a collection of 91 neutral boryl radicals using density functional calculations. Their reactivities were characterized by four indices, i.e., the global electrophilicity, global nucleophilicity, local electrophilicity, and local nucleophilicity. Particularly, the global electrophilicity and nucleophilicity indices span over a moderately wider range than those of carbon radicals, indicating their potentially broader reactivity. Thus, boryl radicals may be utilized in electrophilic radical reactions, while traditionally they are only considered for nucleophilic radical reactions. In contrast, the local electrophilicity and nucleophilicity indices at the boron center show a different reactivity picture than their global counterparts. The inconsistency is rooted in the low and varying spin density on boron (for most radicals, less than 50%) in different boryl radicals, which is a combinative result of radical stabilization via electron delocalization and the low electronegativity of boron (compared to carbon). In short, the boron character in boryl radicals may be weak and their reactivity is not reflected by the local indices based on boron but by the global ones. [GRAPHICS]
引用
收藏
页码:2898 / 2905
页数:8
相关论文
共 50 条
  • [21] Prediction of Nucleophilicity and Electrophilicity Based on a Machine-Learning Approach
    Liu, Yidi
    Yang, Qi
    Cheng, Junjie
    Zhang, Long
    Luo, Sanzhong
    Cheng, Jin-Pei
    CHEMPHYSCHEM, 2023, 24 (14)
  • [22] ELECTROPHILICITY AND NUCLEOPHILICITY IN SINGLET CARBENES .2. ELECTROPHILIC SELECTIVITY
    SCHOELLER, WW
    TETRAHEDRON LETTERS, 1980, 21 (16) : 1509 - 1510
  • [23] Study of humic substance transformation in phosphatic soil in terms of nucleophilicity and electrophilicity
    Kudeyarova, AY
    BIOLOGY BULLETIN, 2006, 33 (03) : 293 - 303
  • [24] SCALES OF NUCLEOPHILICITY AND ELECTROPHILICITY - A SYSTEM FOR ORDERING POLAR ORGANIC AND ORGANOMETALLIC REACTIONS
    MAYR, H
    PATZ, M
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION IN ENGLISH, 1994, 33 (09): : 938 - 957
  • [25] Study of humic substance transformation in phosphatic soil in terms of nucleophilicity and electrophilicity
    A. Yu. Kudeyarova
    Biology Bulletin, 2006, 33 : 416 - 416
  • [26] Using phenyl cations as probes for establishing electrophilicity-nucleophilicity relations
    Dichiarante, Valentina
    Fagnoni, Maurizio
    Albini, Angelo
    JOURNAL OF ORGANIC CHEMISTRY, 2008, 73 (04): : 1282 - 1289
  • [27] Study of humic substance transformation in phosphatic soil in terms of nucleophilicity and electrophilicity
    A. Yu. Kudeyarova
    Biology Bulletin, 2006, 33 : 293 - 303
  • [28] LIGATED BORYL RADICALS .2. ELECTRON-SPIN RESONANCE STUDIES OF TRIALKYLAMINE BORYL RADICALS
    BABAN, JA
    MARTI, VPJ
    ROBERTS, BP
    JOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 2, 1985, (11): : 1723 - 1733
  • [29] A comparative study to predict regioselectivity, electrophilicity and nucleophilicity with Fukui function and Hirshfeld charge
    Wang, Bin
    Rong, Chunying
    Chattaraj, Pratim K.
    Liu, Shubin
    THEORETICAL CHEMISTRY ACCOUNTS, 2019, 138 (12)
  • [30] Understanding local electrophilicity/nucleophilicity activation through a single reactivity difference index
    Chattaraj, Pratim K.
    Duley, Soma
    Domingo, Luis R.
    ORGANIC & BIOMOLECULAR CHEMISTRY, 2012, 10 (14) : 2855 - 2861