Abstract
Protonolysis, complex-formation with amines, ab initio molecular orbital calculations with 3-21G basis set, redox potentials, and spectroscopic features of 1-phenylthieno[3,4-d]borepin (1) and 1-phenylthieno[2,3-d]borepin (2) were examined. The compound 1 was shown to be more labile than 2, which give us a guide for construction of stable heteroaromatics. Absorption and fluorescence spectra of 1 and 2 revealed the potential ability of boron heterocycles in the field of the organic optical materials.
Original language | English |
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Pages (from-to) | 6495-6504 |
Number of pages | 10 |
Journal | Tetrahedron |
Volume | 50 |
Issue number | 22 |
DOIs | |
State | Published - 1994 |
ASJC Scopus subject areas
- Biochemistry
- Drug Discovery
- Organic Chemistry