Issue 14, 2012

Cucurbit[8]uril-stabilized charge transfer complexes with diquat driven by pH: a SERS study

Abstract

In this work, we have studied the pH-dependence of the formation of DQCB[8] complexes by surface-enhanced Raman scattering (SERS) spectroscopy. The SERS spectra suggest that at acidic pH CB[8] can form a binary complex with the dication DQ+2 while at higher pH ternary complexes with the radical cation dimer (DQ+˙)2 and the radical cation–dication dimer (DQ+˙DQ+2) are formed. The pH-enhanced diquat (DQ) dimerization inside the cucurbit[8]uril cavity has not been reported until now. In addition, this study provides very valuable information regarding the use of CB[8] functionalized silver nanoparticles as SERS substrate for sensing applications.

Graphical abstract: Cucurbit[8]uril-stabilized charge transfer complexes with diquat driven by pH: a SERS study

Supplementary files

Article information

Article type
Paper
Submitted
07 Nov 2011
Accepted
24 Jan 2012
First published
26 Jan 2012

Phys. Chem. Chem. Phys., 2012,14, 4935-4941

Cucurbit[8]uril-stabilized charge transfer complexes with diquat driven by pH: a SERS study

M. L. Roldán, S. Sanchez-Cortes, J. V. García-Ramos and C. Domingo, Phys. Chem. Chem. Phys., 2012, 14, 4935 DOI: 10.1039/C2CP23503J

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