How strong is a pi-facial hydrogen bond?

被引：67

作者：

Adams, H

Harris, KDM

Hembury, GA

Hunter, CA

Livingstone, D

McCabe, JF

机构：

[1] UNIV BIRMINGHAM,SCH CHEM,BIRMINGHAM B15 2TT,W MIDLANDS,ENGLAND

[2] SMITHKLINE BEECHAM,WELWYN GARDEN CIT AL6 9AR,HERTS,ENGLAND

来源：

CHEMICAL COMMUNICATIONS | 1996年 / 22期

关键词：

D O I：

10.1039/cc9960002531

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

Functional group substitutions (chemical mutations) in a molecular zipper complex have been used to construct a thermodynamic cycle for estimating the strength of a pi-facial H-bond between an NH group and an aromatic ring resulting in a lower limit of -4.5 +/- 0.5 kJ mol(-1) for the magnitude of the intermolecular NH-pi interaction in chloroform.

引用

页码：2531 / 2532

页数：2

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