Literature DB >> 12659550

Exploiting the versatile assembly of arylpyridine fluorophores for wavelength tuning and SAR.

Albert G Fang1, Jesse V Mello, Nathaniel S Finney.   

Abstract

[reaction: see text] The facile modular assembly of polyarylpyridine fluorophores provides two important advantages in the development of fluorescent chemosensors: it allows rapid dissection of the structural requirements for fluorescent chemosensing and it allows dramatic tuning of emission wavelength by changes in a substituent remote from the binding site.

Entities:  

Year:  2003        PMID： 12659550     DOI： 10.1021/ol0272287

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

1.  Spermine detection via metal-mediated ethynylarene 'turn-on' fluorescence signaling.

Authors:  James T Fletcher; Brent S Bruck
Journal:  Sens Actuators B Chem       Date:  2015-02-01       Impact factor: 7.460

2.  2-(1,2,3-Triazol-4-yl)pyridine-containing ethynylarenes as selective 'turn-on' fluorescent chemosensors for Ni(II).

Authors:  Joseph A Christensen; James T Fletcher
Journal:  Tetrahedron Lett       Date:  2014-08-01       Impact factor: 2.415

3.  Dicarboxylated ethynylarenes as buffer-dependent chemosensors for Cd(II), Pb(II) and Zn(II).

Authors:  James T Fletcher; Brent S Bruck; Douglas E Deever
Journal:  Tetrahedron Lett       Date:  2013-09-25       Impact factor: 2.415

4.  Some mechanistic aspects regarding the Suzuki-Miyaura reaction between selected ortho-substituted phenylboronic acids and 3,4,5-tribromo-2,6-dimethylpyridine.

Authors:  Piotr Pomarański; Piotr Roszkowski; Jan K Maurin; Armand Budzianowski; Zbigniew Czarnocki
Journal:  Beilstein J Org Chem       Date:  2018-09-11       Impact factor: 2.883
  4 in total

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