Issue 83, 2014
From the journal:

RSC Advances

Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols†

Massimiliano Cordaro,*a   Placido Mineo,bc   Francesco Nastasia  and  Giuseppe Magazzùa  

* Corresponding authors

a Dipartimento di Scienze Chimiche, Università di Messina, Viale F. Stagno D'Alcontres, 31, 98166 Messina, Italy
E-mail: mcordaro@unime.it
Fax: +39 090 393895
Tel: +39 090 6765511

b Dipartimento di Scienze Chimiche, Università di Catania, I.N.S.T.M. UdR of Catania, Viale A. Doria 6, 95125 Catania, Italy

c CNR-IPCF Istituto per i Processi Chimico Fisici, Viale Ferdinando Stagno D'Alcontres, 37, 98158 Messina, Italy

Abstract

An efficient strategy for the synthesis of o-((ethyl)aminomethyl) phenyl boronic acid anchored on a BODIPY core is reported. Kinetic studies highlight the association with diols and fructose; BODIPY fluorescence is quenched upon substrate binding, showing an unusual turn-off response.

Graphical abstract: Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols

About
Cited by
Related
Download options Please wait...

Supplementary files

Article information

DOI
https://doi.org/10.1039/C4RA08213C
Article type
Communication
Submitted
06 Aug 2014
Accepted
10 Sep 2014
First published
16 Sep 2014

RSC Adv., 2014,4, 43931-43933

Permissions

Request permissions

Facile synthesis of boronic acids on a BODIPY core with promising sensitivity towards polyols

M. Cordaro, P. Mineo, F. Nastasi and G. Magazzù, RSC Adv., 2014, 4, 43931 DOI: 10.1039/C4RA08213C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements