Demonstrating a New Valence-Bond Interpretation ofConjugation in Polycyclic Conjugated Hydrocarbons with a Single Kekule Structure

被引:1
|
作者
Dias, Jerry Ray [1 ]
机构
[1] Univ Missouri, Dept Chem, 5100 Rockhill Rd, Kansas City, MO 64110 USA
关键词
conjugation; Dewar resonance structures; polyene hydrocarbons; resonance-theoretic analysis; valence-bond; COMPUTER-GENERATION; CHEMICAL GRAPHS; LENGTHS; POLYNOMIALS; ORDERS;
D O I
10.1080/10406638.2015.1028589
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
For polyene molecules with a single classical structure, those with more double bonds and more rings have more Dewar resonance structures. The more Dewar resonance structures a polyene has the more it is conjugated and stable. These generalizations are illustrated by comparing sets of molecules with the same number of fixed double bonds. A step-by-step algorithm for rapidly determining the number of Dewar resonance structures in small typical conjugated polyenes is given. Some new analytical equations for the number of Dewar resonance structures (DS) for series of pyrene-related conjugated polyenes with a single classical structure are also presented. Some general qualitative rules for evaluating relative order of conjugation in polyenes are summarized.
引用
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页码:544 / 553
页数:10
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