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Theoretical investigations of the aromaticity, stability and photophysical behaviors for expanded porphyrins

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成果类型:
期刊论文
作者:
Wei, Wei;Li, Wei;Xia, Bao-Hui*;Zhang, Hong-Xing;Bai, Fu-Quan*
通讯作者:
Xia, Bao-Hui;Bai, Fu-Quan
作者机构:
[Xia, Bao-Hui; Bai, Fu-Quan; Wei, Wei; Zhang, Hong-Xing] Jilin Univ, Inst Theoret Chem, Lab Theoret & Computat Chem, Changchun 130012, Jilin, Peoples R China.
[Li, Wei] Hunan Agr Univ, Coll Sci, Changsha 410128, Hunan, Peoples R China.
[Xia, Bao-Hui] Jilin Univ, Coll Chem, Changchun 130023, Jilin, Peoples R China.
通讯机构:
[Xia, BH; Bai, FQ; Xia, Bao-Hui] J
Jilin Univ, Inst Theoret Chem, Lab Theoret & Computat Chem, Changchun 130012, Jilin, Peoples R China.
Jilin Univ, Coll Chem, Changchun 130023, Jilin, Peoples R China.
语种:
英文
关键词:
Aromaticity;DFT;Expanded porphyrins;Photophysical behaviors;Stability
期刊:
Chemical Physics Letters
ISSN:
0009-2614
年:
2019
卷:
728
页码:
25-31
基金类别:
The present work calculates the aromaticity, stability, and photophysical properties of 1–8 through theoretical calculations. Compounds 1–8 show high aromaticity and good photophysical properties. Both the HOMO-LUMO gaps (ΔH-L) values the NICS values are used to evaluate the stability for 1–8. Compared with the molecule with DTT, the molecule with 2,2′-bithiophene is more stable. The sapphyrins with a thiophene ring or selenophene ring are more stable than the ones with an inverted thiophene
机构署名:
本校为其他机构
院系归属:
理学院
摘要:
We design a series of expanded porphyrins which are incorporated of dithienothiophene (DTT), 2,2′-bithiophene, inverted thiophene ring or selenophene ring and substituted of the pyrrole NH groups by S and Se heteroatoms. The molecule with 2,2′-bithiophene is more stable than the molecule with DTT. The expanded porphyrins with a thiophene or selenophene ring are more stable than the expanded porphyrins with an inverted thiophene or inverted selenophene ring. 6 shows special features due to its increased HOMO-LUMO gap, planar geometry, and stre...

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