2012
DOI: 10.1021/ol302347m
|View full text |Cite
|
Sign up to set email alerts
|

Large Stokes Shift Induced by Intramolcular Charge Transfer in N,O-Chelated Naphthyridine–BF2 Complexes

Abstract: Novel N,O-chelated naphthyridine-BF(2) complexes with push-pull structures have been synthesized and characterized. Spectral investigations on these complexes reveal that photoinduced intramolecular charge transfer occurs and results in a large Stokes shift, which is further supported by density functional theory based theoretical calculations.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

7
40
0
2

Year Published

2013
2013
2024
2024

Publication Types

Select...
6
1

Relationship

0
7

Authors

Journals

citations
Cited by 132 publications
(49 citation statements)
references
References 35 publications
7
40
0
2
Order By: Relevance
“…The theoretical simulated trend of S-Q and S-R is in accordance with the experiment. A large stokes shift can be induced by an excellent ICT property [60,61]. Accordingly, the shorter stokes shift of S-Q demonstrates that S-Q has a low ICT performance.…”
Section: Polarizability First Hyperpolarizability and Charge Transfementioning
confidence: 99%
“…The theoretical simulated trend of S-Q and S-R is in accordance with the experiment. A large stokes shift can be induced by an excellent ICT property [60,61]. Accordingly, the shorter stokes shift of S-Q demonstrates that S-Q has a low ICT performance.…”
Section: Polarizability First Hyperpolarizability and Charge Transfementioning
confidence: 99%
“…However most of the reported difluoroboron complexes show very small stokes shifts and hardly show any solid state fluorescence. In recent years new class difluoroboron complexes such as boron-diketonates [15][16][17], anilin imines (anils) and/or moieties containing b-iminoenolate ligands with improved properties as solid state fluorescence, sensitivity upon changes in polarity of the microenvironment and aggregation induced http fluorescence [4,15,[18][19][20][21][22] have been developed. The difluoroboron complex of curcumin was initially developed with increased stability and inhibitory potency against HIV protease [23].…”
Section: Introductionmentioning
confidence: 99%
“…Absorption maxima ( λ abs ) are in the range of 505–535 nm, with a progressive blue shift as the polarity of the medium increases. Fluorescence maxima ( λ em ) are in the 660–725 nm range; more polar media lead to a red shift, consistent with an excited state with intramolecular charge transfer characteristics . Fluorescence quantum efficiencies ( Φ F ) were also measured in different solvents.…”
Section: Methodsmentioning
confidence: 84%