Citation

BibTex format

@article{Ugolotti:2007:10.1039/b700317j,
author = {Ugolotti, J and Hellstrom, S and Britovsek, GJP and Jones, TS and Hunt, P and White, AJP},
doi = {10.1039/b700317j},
journal = {Dalton Trans},
pages = {1425--1432},
title = {Synthesis and characterisation of luminescent fluorinated organoboron compounds.},
url = {http://dx.doi.org/10.1039/b700317j},
year = {2007}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - The reaction of 8-hydroxyquinoline (HQ) with B(C(6)F(5))(3) leads to the formation of the zwitterionic compound (C(6)F(5))(3)BQH (1), involving a proton migration from O to N. Compound 1 can be converted thermally to (C(6)F(5))(2)BQ (2), which can also be prepared from (C(6)F(5))(2)BCl and HQ. The reaction of HQ with (C(6)F(5))B(OC(6)F(5))(2) generates initially (C(6)F(5))(OC(6)F(5))BQ (3), which easily hydrolyses to give the diboron compound ((C(6)F(5))BQ)(2)O (4). Compounds 1, 2 and 4 have been fully characterised, including X-ray analysis. The spectroscopic properties of these compounds, including photoluminescence (PL) have been investigated and compared with the non-fluorinated luminescent boron compound (C(6)H(5))(2)BQ and also with AlQ(3). The changes in luminescent behaviour upon fluorination of these boron quinolinate compounds have been rationalised using computational studies.
AU - Ugolotti,J
AU - Hellstrom,S
AU - Britovsek,GJP
AU - Jones,TS
AU - Hunt,P
AU - White,AJP
DO - 10.1039/b700317j
EP - 1432
PY - 2007///
SN - 1477-9226
SP - 1425
TI - Synthesis and characterisation of luminescent fluorinated organoboron compounds.
T2 - Dalton Trans
UR - http://dx.doi.org/10.1039/b700317j
UR - https://www.ncbi.nlm.nih.gov/pubmed/17387404
ER -