Issue 44, 2012

Propylamino-connected fluorescent terpyridine dimer and trimer: syntheses, photophysical properties and formation of duplex-type complexes with Cd(ii)

Abstract

By using propylamine as a connector, a dimer (L2) and trimer (L3) of 2,2′:6′,2′′-terpyridine (tpy) are synthesized. They showed the lowest energy π–π* absorption at 354 nm and blue fluorescence at 420 nm with a moderate quantum yield in solution. Spectral titrations, electrospray ionization mass spectrometry (ESI-MS), 1H–1H rotating-frame nuclear Overhauser effect correlation spectroscopy (ROESY), and structure simulation (MOPAC/PM5) indicated that both L2 and L3 form duplex-type multi-component complexes with Cd(II), [Cd2(L2)2]4+ and [Cd3(L3)2]6+, respectively. While the luminescence of these complexes was quite weak in solution (quantum yield Φ < 0.005), the complexes showed enhanced emission in the solid state with remarkable increase of the quantum yield (Φ = 0.13).

Graphical abstract: Propylamino-connected fluorescent terpyridine dimer and trimer: syntheses, photophysical properties and formation of duplex-type complexes with Cd(ii)

Supplementary files

Article information

Article type
Paper
Submitted
19 Jun 2012
Accepted
14 Sep 2012
First published
17 Sep 2012

Org. Biomol. Chem., 2012,10, 8895-8902

Propylamino-connected fluorescent terpyridine dimer and trimer: syntheses, photophysical properties and formation of duplex-type complexes with Cd(II)

Y. Kamoya, K. Kojima, G. Tanaka, R. Tanaka, T. Mutai and K. Araki, Org. Biomol. Chem., 2012, 10, 8895 DOI: 10.1039/C2OB26609A

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