Zobrazeno 1 - 10
of 29
pro vyhledávání: '"Prasanta K Hota"'
Publikováno v:
Journal of Fluorescence. 31:51-61
2-substituted thiophene compounds with electron donating and electron withdrawing p-phenyl substitution were synthesized and studied their radical scavenging properties using DPPH assay and DFT method. It is shown that p-hydroxy and p-amino phenyl su
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::72c0625dd7327e46ecf8f104c63a92fd
https://doi.org/10.1007/s10895-020-02629-5
https://doi.org/10.1007/s10895-020-02629-5
Publikováno v:
RSC Advances. 10:28213-28224
The optical properties of various donor or acceptor p-phenyl substituted ethenyl indoles were studied in solvents of varying polarity using absorption, fluorescence and TDDFT methods. Ethenyl indole exhibits non-linear optical properties (NLO) in a s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca52650fa05140f3a173084ff0dcedf2
https://doi.org/10.1039/d0ra05405d
https://doi.org/10.1039/d0ra05405d
Publikováno v:
New Journal of Chemistry. 44:8960-8970
A series of ethenyl indoles (e.g. 3-(4-substituted phenylethenyl-E)-N–H-indole) with various donor or acceptor substituents have been synthesized and their antioxidant properties have been studied. Ethenyl indoles exhibit antioxidant activity in a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3bfb8d2fe96076bacc10f292ab80d46d
https://doi.org/10.1039/d0nj01317j
https://doi.org/10.1039/d0nj01317j
Publikováno v:
Journal of Fluorescence. 28:1207-1216
Various electron donor and acceptor substituted (NO2, CN, Cl, H, OCH3, NH2) p-phenyl ethenyl-E- thiophenes (1–6) were synthesized and substituent dependent optical properties (dipole moment, transition dipole moment, oscillator strength, optical ba
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bea8cdca2e376f7cc04c6c2989675da8
https://doi.org/10.1007/s10895-018-2284-6
https://doi.org/10.1007/s10895-018-2284-6
Publikováno v:
Letters in Organic Chemistry. 15:479-484
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e55de2a49d1ceb1aac8b3ab7edda4285
https://doi.org/10.2174/1570178614666171129161030
https://doi.org/10.2174/1570178614666171129161030
Autor:
Stephanie Black, Prasanta K. Hota, Sejal Doshi, Aaron Prodeus, Richard M. Epand, William Jennings
Publikováno v:
Biochemistry. 56:1337-1347
Diacylglycerol kinase ε (DGKε) catalyzes the phosphorylation of diacylglycerol, producing phosphatidic acid. DGKε demonstrates exquisite specificity for the acyl chains of diacylglycerol. This contributes to the enrichment of particular acyl chain
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ebc3d404fe5382a58f45b8e01d57307
https://doi.org/10.1021/acs.biochem.6b01193
https://doi.org/10.1021/acs.biochem.6b01193
Autor:
P. Ravi Kumar, Satyanarayana Yennam, K. Raghavulu, Loka Reddy Velatooru, Siva Reddy Kotla, Vasudevarao Penugurti, Prasanta K Hota, Manoranjan Behera, A. Jaya Shree
Publikováno v:
Drug research.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca70ccf52b8a15f9974f23374096f634
https://pubmed.ncbi.nlm.nih.gov/30722080
https://pubmed.ncbi.nlm.nih.gov/30722080
Publikováno v:
Journal of Luminescence. 230:117725
2-(p-phenyl substituted styryl)-furans were synthesized and studied the excited state and anti oxidation properties using absorption, fluorescence, density functional theory and DPPH radical scavenging assay. 2-(p-hydroxy phenyl styryl)-furan (6) exh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b8644f4d6878302e1ed717719c7b2d6
https://doi.org/10.1016/j.jlumin.2020.117725
https://doi.org/10.1016/j.jlumin.2020.117725
Publikováno v:
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy. 206
p-Phenyl ethenyl-E-furans (1–6) with varied electron donor and acceptor substituent (NO2, CN, Cl, H, OCH3, NH2) were synthesized and studied the substituent induced optical properties (dipole moment, transition dipole moment, oscillator strength, o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfdb4dc44f4e325dc26cd0f70a46445e
https://pubmed.ncbi.nlm.nih.gov/30172237
https://pubmed.ncbi.nlm.nih.gov/30172237
Publikováno v:
Journal of fluorescence. 27(5)
Donor-acceptor conjugated molecules with efficient light induced properties represent interesting material for electronic device application. In this context, we have calculated excited state dipole moment of three ethenyl thiophenes (1-3) bearing va
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::914a746c90810721772620ea0f413fb2
https://pubmed.ncbi.nlm.nih.gov/28477137
https://pubmed.ncbi.nlm.nih.gov/28477137