z-logo
Premium
Synthesis and Photophysical Studies of Calixarene‐Based Alkynylplatinum(II) Terpyridine Complexes with Various Receptor Sites for Colorimetric and Luminescence Sensing of Anions
Author(s) -
Hau Franky KaWah,
Lo HiuSuet,
Yam Vivian WingWah
Publication year - 2016
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201503401
Subject(s) - chemistry , terpyridine , stacking , luminescence , amide , intramolecular force , ion , absorption (acoustics) , calixarene , absorption spectroscopy , photochemistry , proton nmr , stereochemistry , crystallography , molecule , metal , organic chemistry , materials science , physics , optoelectronics , quantum mechanics , composite material
A series of mononuclear and dinuclear platinum(II) terpyridine complexes with amide‐, sulfonamide‐, and urea‐containing ligands ( 1 – 9 ) has been successfully designed and synthesized, and their photophysical and anion‐binding properties have been studied. The anion‐binding properties of the complexes were studied by electronic absorption, emission, and 1 H NMR spectroscopy. Upon the binding with anions, the dinuclear complexes 1 – 3 exhibit large electronic absorption and emission spectral changes, while for the mononuclear analogues 4 – 6 much smaller spectral changes were observed. Interesting colorimetric responses towards different anions were observed in dinuclear complexes 1 – 3 . Dinuclear complexes 7 – 9 are found to be insensitive to anion‐binding, which could be attributed to the presence of intramolecular Pt⋅⋅⋅Pt interactions and/or π–π stacking in the complexes that led to the reduced anion‐binding affinity.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom