A Stable Push-Pull Disilene: Substantial Donor-Acceptor Interactions through the Si=Si Double Bond

被引:0
|
作者
Kosai, Tomoyuki
Iwamoto, Takeaki
机构
关键词
Organic compounds;
D O I
暂无
中图分类号
学科分类号
摘要
The push-pull effect has been widely used to effectively tune π-electron systems. Herein, we report the synthesis and properties of 1-amino-2-boryldisilene 1 as the first push-pull disilene. Its spectroscopic and structural features show substantial interactions between the Si=Si double bond and the amino and boryl substituents. The π→ π∗ absorption band of 1 is remarkably red-shifted compared to that of the corresponding alkyl-substituted disilene 2. Treatment of 1 with H2 resulted in the cleavage of two molecules of H2 under concomitant formation of the corresponding trihydridodisilane and hydroborane. © 2017 American Chemical Society.
引用
收藏
相关论文
共 44 条
  • [21] Influence of push-pull group substitution patterns on excited state properties of donor-acceptor co-monomers and their trimers
    de Gier, Hilde D.
    Rietberg, Bernd J.
    Broer, Ria
    Havenith, Remco W. A.
    COMPUTATIONAL AND THEORETICAL CHEMISTRY, 2014, 1040 : 202 - 211
  • [22] Grafting small organic molecules on donor-acceptor polymers to regulate electron push-pull interactions for efficient H2O2 production
    Zhao, Shuang
    Li, Najun
    Xu, Qingfeng
    Li, Hua
    Lu, Jianmei
    Chen, Dongyun
    CHEMICAL ENGINEERING JOURNAL, 2024, 488
  • [23] Efficient generation of stable adducts of Si(II) dihydride using a donor-acceptor approach
    Al-Rafia, S. M. Ibrahim
    Malcolm, Adam C.
    McDonald, Robert
    Ferguson, Michael J.
    Rivard, Eric
    CHEMICAL COMMUNICATIONS, 2012, 48 (09) : 1308 - 1310
  • [24] PUSH-PULL SUBSTITUTED ALLENES .7. VINYL THIOETHERS AND THIOKETONES FROM DONOR-ACCEPTOR SUBSTITUTED ALLENES AND ELEMENTAL SULFUR
    SAALFRANK, RW
    PAUL, W
    SCHIERLING, P
    SCHULER, H
    WILHELM, E
    CHEMISCHE BERICHTE-RECUEIL, 1982, 115 (01): : 57 - 64
  • [25] Vibrational Spectroscopy Reveals Effects of Electron Push-Pull and Solvent Polarity on Electron Delocalization in Radical Anions of Donor-Acceptor Compounds
    Boudreau, Andrew M.
    Wilson, Reid W.
    Yang, Mengshijie
    Grills, David C.
    Mani, Tomoyasu
    JOURNAL OF PHYSICAL CHEMISTRY B, 2020, 124 (08): : 1543 - 1549
  • [26] Resonance hyper-Raman scattering from conjugated organic donor-acceptor "push-pull" chromophores with large first hyperpolarizabilities
    Kelley, AM
    Leng, WN
    Blanchard-Desce, M
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2003, 125 (35) : 10520 - 10521
  • [28] PHOTOPHYSICS OF LINKED DONOR-ACCEPTOR SYSTEMS - THROUGH-SPACE AND THROUGH-BOND INTERACTIONS
    DESCHRYVER, FC
    DECLERCQ, D
    DEPAEMELAERE, S
    HERMANS, E
    ONKELINX, A
    VERHOEVEN, JW
    GELAN, J
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1994, 82 (1-3) : 171 - 179
  • [29] Nanographene favors electronic interactions with an electron acceptor rather than an electron donor in a planar fused push-pull conjugate
    Volland, Michel
    Zhou, Ping
    Wibmer, Leonie
    Haener, Robert
    Decurtins, Silvio
    Liu, Shi-Xia
    Guldi, Dirk M.
    NANOSCALE, 2019, 11 (03) : 1437 - 1441
  • [30] Spectral Properties of Y-Shaped Donor-Acceptor Push-Pull Imidazole-based Fluorophores: Comparison between Solution and Polymer Matrices
    Martin Danko
    Filip Bureš
    Jiří Kulhánek
    Pavol Hrdlovič
    Journal of Fluorescence, 2012, 22 : 1165 - 1176