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篇目详细内容 |
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【篇名】 |
Photochromic reactions of 6-hydroxy-5,12-naphthacenequinone and its derivatives bearing methyl or phenyl groups |
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【刊名】 |
Frontiers of Chemistry in China |
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【刊名缩写】 |
Front. Chem. China |
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【ISSN】 |
1673-3495 |
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【EISSN】 |
1673-3614 |
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【DOI】 |
10.1007/s11458-008-0072-6 |
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【出版社】 |
Higher Education Press and Springer-Verlag |
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【出版年】 |
2008 |
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【卷期】 |
3
卷4期 |
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【页码】 |
400-405
页,共
6
页 |
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【作者】 |
YIN Jinghua;
LIAN Huiqin;
ZHAO Jiyang;
WU Xue;
ZHOU Ziyan;
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【关键词】 |
naphthacenequinone; photochromism; photoisomerization; density functional theory; electronic spectra |
【摘要】 |
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Photoisomerizations of 6-hydroxy-5,12-naphthacenequinone and its derivatives bearing methyl and phenyl group were theoretically investigated with density functional theory and ab initio CIS method at the B3LYP 6-31G basis set, respectively. The obtained potential energy curves revealed that a four-state cycle existed in the ground and excited states. It was also found that the activation energy for the methyl transfer was higher compared to that for the phenyl transfer, and this was consistent with the experimental results that the photoisomerization of the phenyl substituted derivative was more rapid than that of the methyl substituted derivatives. Further hybrid time-dependent density functional theory (TD-DFT) was used to investigate the absorption and fluorescence spectra of these compounds under solvent effect condition. The calculated values were in agreement with the experimental results and the excitation condition of photochromic reactions. |
