Intrinsic relative nucleophilicity of indoles

被引:6
|
作者
Chamorro, Eduardo [1 ]
Duque-Norena, Mario [1 ]
Rios-Gutierrez, Mar [2 ]
Domingo, Luis R. [2 ]
Perez, Patricia [1 ]
机构
[1] Univ Andres Bello, Fac Ciencias Exactas, Dept Ciencias Quim, Millennium Nucleus Chem Proc & Catalysis CPC, Ave Republ 275, Santiago 8370146, Chile
[2] Univ Valencia, Dept Quim Organ, Dr Moliner 50, E-46100 Valencia, Spain
关键词
Nucleophilicity; Electrophilicity; Conceptual DFT; Indoles; Reactivity Scales; Polar organic reactions; QUANTITATIVE CHARACTERIZATION; CHEMICAL-REACTIVITY; EXPERIMENTAL-MODELS; FUKUI FUNCTION; ELECTROPHILICITY; SCALES; INDEX; FUNCTIONALIZATION; PARAMETERS; HARDNESS;
D O I
10.1007/s00214-016-1974-x
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The range of applicability of intrinsic (i.e., electronic) relative indices for quantifying electrophilicity and nucleophilicity responses (Chamorro et al. in J Phys Chem A 117(12): 2636-2643, 2013) is extended to the characterization of coupling reactions of indoles with benzhydrylium ions and with the strongly electron-deficient heteroarene 4,6-dinitrobenzofuroxan. The reactivity categorization based on experimental kinetic evidence for such a electrophile/nucleophile coupling (Lakhdar et al. in J Org Chem 71(24): 9088-9095, 2006) is rationalized in terms of purely electronic descriptors, revealing the polar nucleophilic activation of indole as a key factor associated with the initial rate-determining C-C coupling process.
引用
收藏
页数:12
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