Zobrazeno 1 - 10
of 176
pro vyhledávání: '"Samaresh Bhattacharya"'
Autor:
Jit Karmakar, Promita Nandy, Saurabh Das, Debalina Bhattacharya, Parimal Karmakar, Samaresh Bhattacharya
Publikováno v:
ACS Omega, Vol 6, Iss 12, Pp 8226-8238 (2021)
Externí odkaz:
https://doaj.org/article/4bd2ab8a43174e0d86419cc43eaa25ba
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
Reaction of [Rh(PPh3)3Cl] with two Schiff base ligands, viz. N-(2′-hydroxyphenyl)furan-2-aldimine (H2L1) and N-(2′-hydroxyphenyl)thiophene-2-aldimine (H2L2), in refluxing toluene affords organorhodium complexes of type [Rh(PPh3)2(L)Cl] (L = L1 an
Externí odkaz:
https://doaj.org/article/fc49075d52f64a94a5f92ad66ff38e2c
Publikováno v:
New Journal of Chemistry. 47:3492-3501
Reaction of N-(4′-R-phenyl)pyrrole-2-aldimines (HL-R) with [Ru(dmso)4Cl2] in refluxing toluene affords complexes of type [Ru(L-R)2(dmso)2]. The two dmso's can be substituted by a chelating bidentate ligand such as bpy (or phen).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::308fd65b711798882938221074d7b24c
https://doi.org/10.1039/d2nj05295d
https://doi.org/10.1039/d2nj05295d
Publikováno v:
New Journal of Chemistry. 46:9098-9110
A ruthenium(ii)–aquo complex serves as a precursor for the synthesis of new ternary complexes and also as an efficient catalyst for selective hydration of aryl nitriles to aryl amides and aryl alkynes to aryl aldehydes.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::33d044c035d067e511d4d03e2b2a7b3e
https://doi.org/10.1039/d1nj04736a
https://doi.org/10.1039/d1nj04736a
Autor:
Piyali Paul, Samaresh Bhattacharya
Department of Chemistry and Environment, Heritage Institute of Technology, Kolkata-700 107, India Department of Chemistry, Inorganic Chemistry Section, Jadavpur University, Kolkata-700 032, India E-mail: samareshb. chemistry@j adavpuruni versity. in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c2138d513344e0301febe8f7a200953e
Autor:
Parimal Karmakar, Debalina Bhattacharya, Saurabh Das, Promita Nandy, Samaresh Bhattacharya, Jit Karmakar
Publikováno v:
ACS Omega
ACS Omega, Vol 6, Iss 12, Pp 8226-8238 (2021)
ACS Omega, Vol 6, Iss 12, Pp 8226-8238 (2021)
A family of three water-soluble half-sandwich arene-ruthenium complexes, depicted as C1 -C3 , having the general formula [Ru(p-cymene)(L)Cl]Cl has been synthesized, where L represents (1H-benzo[d]imidazol-2-yl)guanidine (L1 ) or (benzo[d]oxazol-2-yl)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f68af93e7b34bc450228760f94a6413
http://europepmc.org/articles/PMC8015125
http://europepmc.org/articles/PMC8015125
Publikováno v:
European Journal of Inorganic Chemistry. 2020:4539-4548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b0381272c7613c1266a47bcddad5407d
https://doi.org/10.1002/ejic.202000859
https://doi.org/10.1002/ejic.202000859
Publikováno v:
Journal of Molecular and Engineering Materials.
Redox non-innocent organic substrates, viz. 3,5-di-tert-butylcatechol (3,5-DBC) and 2-aminophenol (2-AP), undergo facile aerial oxidation on silica surface to exclusively afford 3,5-di-tert-butyl-1,2-benzoquinone (3,5-DBQ) and 2-amino-3H-phenoxazin-3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e7bdbcf955b12b2c013bbe9dc900fe8
https://doi.org/10.1142/s2251237321400025
https://doi.org/10.1142/s2251237321400025
Autor:
Jit Karmakar, Samaresh Bhattacharya
Publikováno v:
Polyhedron. 172:39-44
Reaction of 2-(arylazo)phenols (HL-R, where H represents the phenolic proton and, R = CH3, H and Cl) with [{Ru(p-cymene)Cl2}2] in the presence of triethylamine affords a group of three reddish-brown complexes of type [Ru(p-cymene)(L-R)Cl] in good yie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d0633de7426a09bb0bd008f7d3d2ed94
https://doi.org/10.1016/j.poly.2019.02.046
https://doi.org/10.1016/j.poly.2019.02.046
Publikováno v:
Inorganica Chimica Acta. 486:232-239
Reaction of 4-R-benzaldehyde thiosemicarbazone (denoted in general as HL-R; where H stands for the dissociable acidic proton and R (R = OCH3, CH3, H, Cl and NO2) for the substituent) with [Pd(dppe)(EtOH)2]2+, generated in situ via interaction of [Pd(
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cb4827d734068e218885906b90406365
https://doi.org/10.1016/j.ica.2018.10.053
https://doi.org/10.1016/j.ica.2018.10.053