Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Komthep Silpcharu"'
Publikováno v:
ACS Omega, Vol 6, Iss 25, Pp 16696-16703 (2021)
Externí odkaz:
https://doaj.org/article/a6512e641ea04fe884e85a4c9e93044d
Autor:
Paitoon Rashatasakhon, Quynh Nguyen Nhu Pham, Komthep Silpcharu, Viwat Vchirawongkwin, Mongkol Sukwattanasinitt
Publikováno v:
Synlett. 33:1335-1340
Two diaryl derivatives of 1,1,4,4-tetracyanobuta-1,3-diene were synthesized for use as colorimetric ion sensors in aqueous media. The key synthetic step involved a [2+2]-cycloaddition/retro-cycloaddition between an electron-rich diarylethyne and elec
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f165a6f5edd410cd218a1f0b3625768
https://doi.org/10.1055/a-1806-6258
https://doi.org/10.1055/a-1806-6258
Autor:
Thanawat Chaiprasert, Supphachok Chanmungkalakul, Yujia Liu, Teeraya Bureerug, Komthep Silpcharu, Masafumi Unno, Liu Xiaogang, Vuthichai Ervithayasuporn, Young-Tae Chang, Paitoon Rashatasakhon
Publikováno v:
Dyes and Pigments. 208:110793
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e24c1e267238e4ea93454104f47c0c3
https://doi.org/10.1016/j.dyepig.2022.110793
https://doi.org/10.1016/j.dyepig.2022.110793
Publikováno v:
Journal of Fluorescence. 29:417-424
A new symmetrical truxene derivative (TP3) containing three dipicolylamino peripheral groups is successfully synthesized in four synthetic steps with an overall yield of 42%. This hydrophilic fluorescent compound exhibits a maximum absorption wavelen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47a82f59a298bfb9ad116c56a111557e
https://doi.org/10.1007/s10895-019-02350-y
https://doi.org/10.1007/s10895-019-02350-y
Publikováno v:
RSC Advances. 9:11451-11458
Novel spirobifluorene derivatives containing two and four sulfonamide groups are successfully synthesized from the commercially available bromo-9,9′-spirobifluorene by Sonogashira couplings. These compounds exhibit an excellent selective fluorescen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e186d58a3a6c3b33b483581647d9bf4b
https://doi.org/10.1039/c9ra00004f
https://doi.org/10.1039/c9ra00004f
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 25, Pp 16696-16703 (2021)
ACS Omega, Vol 6, Iss 25, Pp 16696-16703 (2021)
A novel spirobifluorene derivative bearing two bissulfonamido groups is successfully synthesized by Sonogashira coupling. This compound exhibits a strong fluorescence quenching by Cu(II) ion in a 50% mixture between acetonitrile and 20 mM pH 7.0 N-(2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a998bba4fcc5821b3d7ab5de31228857
https://pubmed.ncbi.nlm.nih.gov/34235342
https://pubmed.ncbi.nlm.nih.gov/34235342
Autor:
Arnupab Kritanusorn, Rungsima Yeetsorn, Costas Tzoganakis, Komthep Silpcharu, Narumol Kreua-ongarjnukool
Publikováno v:
Key Engineering Materials. 757:3-8
The scratch damage resistance and impact strength of PMMA sheets are necessary factors that have to be concerned by manufacturers. The aim of this work is to investigate the influences of silica (Si) from tetraethoxysilane on scratch damage resistanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0cf6132890f87798f7acad49942f59e6
https://doi.org/10.4028/www.scientific.net/kem.757.3
https://doi.org/10.4028/www.scientific.net/kem.757.3
Autor:
Komthep Silpcharu, Mongkol Sukwattanasinitt, Paitoon Rashatasakhon, Kantapat Chansaenpak, Pornpat Sam-ang
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 402:112823
Novel spirobifluorene derivatives bearing two and four sulfonamidopicolyl groups were successfully synthesized by Sonogashira couplings. These strongly emissive compounds showed a good selective fluorescent quenching by Au(III) ion in acidic aqueous
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0160fbd8e8075a9e62cadc7a398517d4
https://doi.org/10.1016/j.jphotochem.2020.112823
https://doi.org/10.1016/j.jphotochem.2020.112823