C
Chettiyam Veettil Suneesh
Researcher at University of Kerala
Publications - 16
Citations - 397
Chettiyam Veettil Suneesh is an academic researcher from University of Kerala. The author has contributed to research in topics: Electron transfer & Radical ion. The author has an hindex of 8, co-authored 14 publications receiving 293 citations. Previous affiliations of Chettiyam Veettil Suneesh include National Institute for Interdisciplinary Science and Technology & Kyushu University.
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Journal ArticleDOI
Cu(II)-mediated generation of triarylamine radical cations and their dimerization. an easy route to tetraarylbenzidines.
Kesavapillai Sreenath,Chettiyam Veettil Suneesh,Venugopal K. Ratheesh Kumar,Karical R. Gopidas +3 more
TL;DR: Synthetic utility of this reaction is demonstrated using several triphenylamine derivatives, and yields in excess of 80% are obtained in most cases, and a mechanism consistent with all observations is proposed.
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Unveiling the compatibility of eugenol with formulation excipients by systematic drug-excipient compatibility studies
TL;DR: The study results confirmed that eugenol is compatible with the selected excipients for the development of nanoemulsion gels and nanoparticles.
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Mechanistic studies of photoinduced intramolecular and intermolecular electron transfer processes in RuPt-centred photo-hydrogen-evolving molecular devices
Chettiyam Veettil Suneesh,Bijitha Balan,Hironobu Ozawa,Yuki Nakamura,Tetsuro Katayama,Masayasu Muramatsu,Yutaka Nagasawa,Hiroshi Miyasaka,Ken Sakai,Ken Sakai +9 more
TL;DR: A key intermediate prior to the H2 formation was found to compete with reductive quenching of the triplet excited state by EDTA whose dianionic form ion-pairs with dicationic RuPt-COOH and some of the conformers in solution possess a CS lifetime sufficiently long to drive hydrogen evolution from water.
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Long-Lived Photoinduced Charge Separation Due to the Inverted Region Effect in 1,6-Bis(phenylethynyl)pyrene-Phenothiazine Dyad
TL;DR: In this paper, photoinduced electron transfer processes in a 1,6-bis (phenylethynyl)pyrene−phenothaiazine dyad, BPEP−PT, were examined using various techniques.
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Generation of Triarylamine Radical Cations through Reaction of Triarylamines with Cu(II) in Acetonitrile. A Kinetic Investigation of the Electron-Transfer Reaction
TL;DR: The high reorganization obtained from these studies is consistent with significant bond cleavage in the transition state, and a mechanism consistent with the experimental data is proposed.