Adaptive σ-Aromaticity in an Unsaturated Three-Membered Ring

被引:19
|
作者
Huang, Yuanyuan [1 ,2 ,3 ]
Dai, Chenshu [1 ,2 ,3 ]
Zhu, Jun [1 ,2 ,3 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, Xiamen 361005, Peoples R China
[2] Xiamen Univ, Collaborat Innovat Ctr Chem Energy Mat IChEM, Xiamen 361005, Peoples R China
[3] Xiamen Univ, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
基金
美国国家科学基金会;
关键词
adaptive aromaticity; sigma-aromaticity; DFT calculations; three-membered ring; excited-state aromaticity; INDEPENDENT CHEMICAL-SHIFTS; POTENTIAL BASIS-SETS; POLARIZATION FUNCTIONS; STATE AROMATICITY; TRIPLET-STATES; EXCITED-STATE; DENSITY; PI; PLANAR; LOWEST;
D O I
10.1002/asia.202000900
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Based on Huckel's and Baird's rules, species are aromatic either in the lowest singlet state (S-0) or the lowest triplet state (T-1) only. Thus, species with adaptive aromaticity (with aromaticity in both the S-0 and T-1 states) is particularly rare. On the other hand, sigma-aromaticity in the T(1)state has been underdeveloped, let alone adaptive sigma-aromaticity. Herein, via various aromaticity indices including NICS, ACID and EDDB, we demonstrate adaptive sigma-aromaticity in an unsaturated three-membered ring, which is a traditional area dominated by pi-aromaticity. The origin of adaptive sigma-aromaticity could be attributed to the excitation mode of the T(1)state formed from out-of-plane pi molecular orbital to the pi* orbitals. Thus the sigma-aromaticity of the three-membered ring in the S-0 state could hold in the T-1 state. Our findings extend the concept of adaptive sigma-aromaticity into three-membered rings and could be useful to further develop the concept of both sigma-aromaticity and adaptive aromaticity.
引用
收藏
页码:3444 / 3450
页数:7
相关论文
共 50 条
  • [21] Experimental and computational studies of α-lactones:: Structure and bonding in the three-membered ring
    Buchanan, JG
    Charlton, MH
    Mahon, MF
    Robinson, JJ
    Ruggiero, GD
    Williams, IH
    JOURNAL OF PHYSICAL ORGANIC CHEMISTRY, 2002, 15 (09) : 642 - 646
  • [22] Ring Enlargement of Three-Membered Heterocycles by Treatment with In Situ Formed Tricyanomethane
    Banert, Klaus
    Chityala, Madhu
    Korb, Marcus
    CHEMISTRY-A EUROPEAN JOURNAL, 2020, 26 (28) : 6158 - 6164
  • [24] A Three-Membered Cyclic Phosphasilene
    Heider, Yannic
    Willmes, Philipp
    Muehlhausen, Daniel
    Klemmer, Lukas
    Zimmer, Michael
    Huch, Volker
    Scheschkewitz, David
    ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2019, 58 (07) : 1939 - 1944
  • [25] Reactivity and Conformation of Systems containing a Three-membered Heterocycle Conjugated with an Unsaturated Group
    Kamernitskii, A.V.
    Turuta, A.M.
    Russian Chemical Reviews, 1982, 51 (09) : 872 - 886
  • [26] Versatility in the Brook Rearrangement for the Selective Ring-Opening of Three-Membered Rings
    Tugny, Coralie
    Zhang, Fa-Guang
    Marek, Ilan
    CHEMISTRY-A EUROPEAN JOURNAL, 2019, 25 (01) : 205 - 209
  • [27] Three-membered beryllium ring, Be3: not just a hydrogen bond acceptor
    Mazumder, Lakhya J.
    Guha, Ankur K.
    PHYSICAL CHEMISTRY CHEMICAL PHYSICS, 2023, 25 (31) : 20947 - 20950
  • [28] Photochemistry of azobenzenophanes with three-membered bridges
    Rottger, D
    Rau, H
    JOURNAL OF PHOTOCHEMISTRY AND PHOTOBIOLOGY A-CHEMISTRY, 1996, 101 (2-3) : 205 - 214
  • [29] Ring strain energies of three-membered silicon, germanium, and tin pnictogenide rings
    Allard, Christina L.
    Gilbert, Thomas M.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2007, 233 : 285 - 285
  • [30] Oxyfunctionalization of CH2-Group Activated by Adjacent Three-Membered Ring
    Sedenkova, Kseniya N.
    Andriasov, Kristian S.
    Kuznetsova, Tamara S.
    Averina, Elena B.
    CURRENT ORGANIC SYNTHESIS, 2018, 15 (04) : 515 - 532