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1 Ergebnisse
1
Antiaromatic Dicyclopenta[ b,g ]/[ a,f ]naphthalene Isomers..:
Tingting Xu (307597)
;
Yi Han (194901)
;
Zhongjin Shen (1678534)
...
https://figshare.com/articles/journal_contribution/Antiaromatic_Dicyclopenta_i_b_g_i_i_a_f_i_naphthalene_Isomers_Showing_an_Open-Shell_Singlet_Ground_State_with_Tunable_Diradical_Character/17096677. , 2021
Link:
https://doi.org/10.1021/jacs.1c06677.s001
RT Journal T1
Antiaromatic Dicyclopenta[ b,g ]/[ a,f ]naphthalene Isomers Showing an Open-Shell Singlet Ground State with Tunable Diradical Character
UL https://suche.suub.uni-bremen.de/peid=base-ftsmithonian:oai:figshare.com:article_17096677&Exemplar=1&LAN=DE A1 Tingting Xu (307597) A1 Yi Han (194901) A1 Zhongjin Shen (1678534) A1 Xudong Hou (4381321) A1 Qing Jiang (197843) A1 Wangdong Zeng (1677259) A1 Pei Wen Ng (11209838) A1 Chunyan Chi (1702024) YR 2021 K1 Biophysics K1 Biochemistry K1 Cell Biology K1 Chemical Sciences not elsewhere classified K1 Physical Sciences not elsewhere classified K1 two relatively stable K1 theoretical calculations confirm K1 shows stronger antiaromaticity K1 electronic absorption spectra K1 different quinoidal structures K1 attracted intensive interest K1 99 kcal mol K1 88 kcal mol K1 antiaromatic dicyclopenta [< K1 expanded indacene isomers K1 >- butyl -< K1 30 % K1 δ K1 6 </ b K1 0 </ sub K1 5 </ b K1 1 </ sup K1 </ sub K1 − 6 K1 − 0 K1 tetra -< K1 globally antiaromatic K1 dicyclopenta [< K1 >- indacene K1 30 years K1 >< sub K1 tert </ K1 g </ K1 f </ K1 e </ K1 successful synthesis K1 reported synthesis K1 localized character K1 high reactivity K1 h nmr K1 first isolation K1 esr measurements K1 delocalized structure K1 >- indacenes K1 48 %) JF https://figshare.com/articles/journal_contribution/Antiaromatic_Dicyclopenta_i_b_g_i_i_a_f_i_naphthalene_Isomers_Showing_an_Open-Shell_Singlet_Ground_State_with_Tunable_Diradical_Character/17096677 LK http://dx.doi.org/https://doi.org/10.1021/jacs.1c06677.s001 DO https://doi.org/10.1021/jacs.1c06677.s001 SF ELIB - SuUB Bremen
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