A BN anthracene mimics the electronic structure of more highly conjugated systems.
Dalton Trans
; 48(8): 2807-2812, 2019 Feb 19.
Article
in En
| MEDLINE
| ID: mdl-30734032
ABSTRACT
9a,9-BN anthracene was synthesized using a simple three-step sequence involving intramolecular electrophilic borylation of 2-benzylpyridines. The same procedure can be applied to yield a number of substituted 9a,9-BN anthracenes. Spectroscopic characterization of the parental compound (UV-photoelectron spectroscopy, UV-vis absorption/emission) shows an electronic structure more similar to that of a larger conjugated system rather than anthracene, the direct all-carbon analogue.
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Language:
En
Journal:
Dalton Trans
Journal subject:
QUIMICA
Year:
2019
Document type:
Article
Affiliation country:
United States