| Literature DB >> 27862420 |
Sven M Elbert1, Philippe Wagner1, Thines Kanagasundaram1, Frank Rominger1, Michael Mastalerz1.
Abstract
Boron-based dyes are attractive synthetic targets due to their large variability of absorption and emission wavelengths. Through Pictet-Spengler cyclizations, followed by oxidation, π-extended boroquinols have been synthesized. During optimization of the reaction conditions, an unusual dearylation has been found and mechanistically investigated. For two of the synthesized boroquinols, mechanochromic effects with bathochromic shifts up to 50 nm were found upon grinding.Entities:
Keywords: boron; conjugation; fluorescence; mechanochromism; reaction mechanisms
Year: 2016 PMID: 27862420 DOI: 10.1002/chem.201604421
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236