Reversing the Bond Length Alternation Order in Conjugated Polyenes by Substituent Effects

被引:2
作者
Yanai, Hikaru [1 ]
Terajima, Yoshihiko [1 ]
Kleemiss, Florian [2 ,3 ]
Grabowsky, Simon [2 ]
Matsumoto, Takashi [1 ]
机构
[1] Tokyo Univ Pharm & Life Sci, Sch Pharm, 1432-1 Horinouchi, Hachioji, Tokyo 1920392, Japan
[2] Univ Bern, Dept Chem Biochem & Pharmaceut Sci, Freiestr 3, CH-3012 Bern, Switzerland
[3] Univ Regensburg, Fac Chem & Pharm, Univ Str 31, D-93053 Regensburg, Germany
基金
瑞士国家科学基金会;
关键词
bond alternations; bond lengths; complementary bonding analysis; polyenes; quantum crystallography; NONLINEAR-OPTICAL PROPERTIES; NATURAL RESONANCE THEORY; X-RAY; PUSH-PULL; AMIDE; CONSTITUTION; DIFFRACTION; COLOR;
D O I
10.1002/chem.202203538
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We have synthesised several push-pull substituted conjugated polyenes and determined their accurate C-C bond lengths and charge-density distributions by utilising quantum crystallographic techniques. In a series of alkene, dienes, and triene bearing two (trifluoromethyl)sulfonyl (triflyl) groups on the terminal carbon atom, unique reversal of the bond-length alternation (BLA) order has been observed. This is a pronounced aberration from the molecular structure predicted by the Lewis-structure-based neutral resonance structure. Such reversal of BLA order has not been observed in push-pull compounds bearing conventional electron-withdrawing groups such as carbonyl and cyano groups instead of triflyl groups. Bonding behaviour of both normal and reversed bond length alternating systems has been revealed by complementary bonding analysis using several bond descriptors based on the experimentally fitted wavefunctions.
引用
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页数:7
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