Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nicha Prigyai"'
Autor:
Yiping Han, Jirawat Trakulmututa, Taweechai Amornsakchai, Supakorn Boonyuen, Nicha Prigyai, Siwaporn Meejoo Smith
Publikováno v:
ACS Omega, Vol 8, Iss 49, Pp 46663-46675 (2023)
Externí odkaz:
https://doaj.org/article/5c10b54f44794da3957502ab4fcf427d
Autor:
Vuthichai Ervithayasuporn, Nicha Prigyai, Mongkol Sukwattanasinitt, Supphachok Chanmungkalakul
Publikováno v:
New Journal of Chemistry. 45:14141-14148
Octasilsesquioxane cages with co-substituent characteristics were synthesized through polyhydrolytic–condensation reactions involving two mixed monomers, namely i-butyl(triethoxysilane) and organotrialkoxysilanes (e.g., phenyl, vinyl, ethyl, propyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bf40d6707be4e60d7e6015f914431b82
https://doi.org/10.1039/d1nj02381k
https://doi.org/10.1039/d1nj02381k
Autor:
Mongkol Sukwattanasinitt, Vuthichai Ervithayasuporn, Supphachok Chanmungkalakul, Sutthiroj Thanyalax, Nicha Prigyai
Publikováno v:
Materials Advances. 1:3358-3368
Cyclic siloxanes conjugated with anthracene (D4An) and pyrene (D4Py) were prepared via Heck coupling reactions of 2,4,6,8-tetramethyl-2,4,6,8-tetravinylcyclotetrasiloxane with 9-bromoanthracene and 1-bromopyrene, respectively. These materials exhibit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5639f9e946037d0c2d48a52f720c02c0
https://doi.org/10.1039/d0ma00476f
https://doi.org/10.1039/d0ma00476f
Autor:
Suda Kiatkamjornwong, Siriporn Jungsuttiwong, Nuttapon Yodsin, Nicha Prigyai, Vuthichai Ervithayasuporn, Supphachok Chanmungkalakul, Masafumi Unno, Jaursup Boonmak, Nobuhiro Takeda
Publikováno v:
Inorganic Chemistry. 58:15110-15117
A coordination complex, lithium hepta(i-butyl)silsesquioxane trisilanolate (1; Li-T7), a stable intermediate in silsesquioxane (SQ) syntheses, was successfully isolated in 65% yield and found to be...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3476475d8db42ccd8cefcf0d28fa8ab1
https://doi.org/10.1021/acs.inorgchem.9b01836
https://doi.org/10.1021/acs.inorgchem.9b01836
Autor:
Suda Kiatkamjornwong, Vuthichai Ervithayasuporn, Nicha Prigyai, Neeraj Saini, Chidchanok Wannasiri
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 358:215-225
A colorimetric and fluorometric hydrazone Schiff’s base derived from dehydroacetic acid by three-steps and high-yield syntheses under green approach employing ethanol as a solvent has been prepared. Multi-analyte sensing for both metal cation (Cu2+
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::382724bc0f47dad5f7611032ef0c0495
https://doi.org/10.1016/j.jphotochem.2018.03.018
https://doi.org/10.1016/j.jphotochem.2018.03.018
Autor:
Vuthichai Ervithayasuporn, Nicha Prigyai, Supphachok Chanmungkalakul, Suda Kiatkamjornwong, Manlika Masik, Sasikarn Hanprasit
Publikováno v:
Chemical Communications. 53:12108-12111
Pyrene functionalized silsesquioxane cages (PySQ) not only provide significant fluorescence from pyrene-pyrene excimers with a very large Stokes shift (Δλ = 143 nm, 69 930 cm-1) in DMSO but also exhibit fluoride capture results coincidentally with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fce11bf77d677298f1d732016f6a98e
https://doi.org/10.1039/c7cc06647c
https://doi.org/10.1039/c7cc06647c
Autor:
Patcharaporn Boonkitti, Sumana Kladsomboon, Suda Kiatkamjornwong, Vuthichai Ervithayasuporn, Nicha Prigyai, Supphachok Chanmungkalakul, Alisa Phuekphong
Publikováno v:
Chemical Science
Anthracene-conjugated octameric silsesquioxane cages thermodynamically display intramolecular excimer formation, which can be used to identify anions through the change of fluorescence.
Anthracene-conjugated octameric silsesquioxane (AnSQ) cages
Anthracene-conjugated octameric silsesquioxane (AnSQ) cages
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f65d5c190ead99eb6f28eecc6e2f9d3
https://pubmed.ncbi.nlm.nih.gov/30429984
https://pubmed.ncbi.nlm.nih.gov/30429984
Autor:
Supphachok Chanmungkalakul, Chidchanok Wannasiri, Suda Kiatkamjornwong, Nicha Prigyai, Neeraj Saini, Vuthichai Ervithayasuporn
Publikováno v:
Journal of Photochemistry and Photobiology A: Chemistry. 385:112038
Four dual optical signalings of fluorescent hydrazone Schiff bases were synthesized from 1,8-naphthalimide hydrazide and substituted furan and thiophene rings, employing ethanol as green solvent. All synthesized molecules can detect F− and CN− wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25725e8258bc12abf6be985c9743829d
https://doi.org/10.1016/j.jphotochem.2019.112038
https://doi.org/10.1016/j.jphotochem.2019.112038