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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 <Title>Antiaromatic Dicyclopenta[ b,g ]/[ a,f ]naphthalene Isomers Showing an Open-Shell Singlet Ground State with Tunable Diradical Character</Title>

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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