Effect of N-α Substitution on the Electropolymerization of N-Substituted Pyrroles: Structure-Reactivity Relationship Studies

被引:22
作者
Kumar, Sunil [1 ]
Krishnakanth, Sada [1 ]
Mathew, Jomon [2 ]
Pomerantz, Zvika [3 ]
Lellouche, Jean-Paul [3 ]
Ghosh, Subrata [1 ]
机构
[1] Indian Inst Technol Mandi, Sch Basic Sci, Mandi 175001, Himachal Prades, India
[2] Natl Inst Adv Ind Sci & Technol A1ST, Nanosyst Res Inst, Tsukuba, Ibaraki 3058568, Japan
[3] Bar Ilan Univ, Inst Nanotechnol & Adv Mat, Nanomat Res Ctr, Dept Chem, IL-52900 Ramat Gan, Israel
关键词
CONDUCTING POLYMERS; CONJUGATED POLYMERS; POLYPYRROLE; ELECTROCHEMISTRY; ELECTROOXIDATION; COMPOSITE; MONOMERS; FILM; SUPERCAPACITORS; MECHANISMS;
D O I
10.1021/jp411098y
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
Structure reactivity relationship (SRR) studies to understand the effect of N-alpha substitution toward electroactive poly(pyrrole) film formation have carefully been performed. To conduct these SRR studies, a selected chemical library of 21 different N-substituted pyrrole derivatives has been developed using the key well-known Clauson-Kass synthetic reaction from corresponding amine precursors. While investigating electropolymerization features of these novel N-substituted pyrroles, we observed that the steric factor due to alpha-substitution, one among other factors, plays the most significant role in preventing electropolymerization of these oxidizable chemical species. Interestingly, even a sterically small chemical group like a CH3 one present at alpha-position is large enough to prevent monomer electropolymerization. Density functional theory calculations were carried out to analyze the polymerization of substituted pyrrole molecules and to understand the effect of N-substituents on electropolymerization toward the formation of functional conductive film. This systematic study paves the way to effectively design the right N-substitution for the obtainment of corresponding modified functional electrodes for further related applications.
引用
收藏
页码:2570 / 2579
页数:10
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