Zobrazeno 1 - 10
of 184
pro vyhledávání: '"Ion Grosu"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 19, Iss 1, Pp 1776-1784 (2023)
Mechanically interlocked molecules (MIMs) have been important synthetic targets in supramolecular chemistry due to their beautiful structures and intriguing properties. We present herein a new synthetic strategy to access [2]rotaxanes, namely active-
Externí odkaz:
https://doaj.org/article/2f3328209ecd44b494b5c53507725eb2
Autor:
Levi Gabrian, Gavril-Ionel Giurgi, Ioan Stroia, Elena Bogdan, Andreea Petronela Crişan, Niculina Daniela Hădade, Ion Grosu, Anamaria Terec
Publikováno v:
Molecules, Vol 27, Iss 23, p 8463 (2022)
The synthesis of some novel donor-acceptor and acceptor-donor-acceptor systems containing a 2,2′-bi[3,2-b]thienothiophene donor block and various electron-accepting units is described alongside their photophysical properties studied using electroch
Externí odkaz:
https://doaj.org/article/654fbe4e197746b6bfa0ba30658fa832
Autor:
Ioan Stroia, Ionuţ -Tudor Moraru, Maria Miclăuş, Ion Grosu, Claudia Lar, Ioana Georgeta Grosu, Anamaria Terec
Publikováno v:
Frontiers in Chemistry, Vol 9 (2021)
In the context of helical chirality, bridging of biphenyl units leads to banister-type compounds and the stability of the resulted atropisomers may increase dramatically if suitable changes are performed in the linker unit that coils around the biphe
Externí odkaz:
https://doaj.org/article/2bdff505c73a4e528d09447d434c23ab
Autor:
Alexandra Bogdan, Ionuț-Tudor Moraru, Pascale Auban-Senzier, Ion Grosu, Flavia Pop, Narcis Avarvari
Publikováno v:
Molecules, Vol 27, Iss 20, p 6926 (2022)
Chiral bis(TTF) diamides have been obtained in good yields (54–74%) from 1,2-cyclohexane-diamine and the corresponding TTF acyl chlorides. The (R,R)-1 and (S,S)-1 enantiomers have been characterized by circular dichroism and the racemic form by sin
Externí odkaz:
https://doaj.org/article/03925c6f45234e2ab3c843588f2efb6b
Autor:
Natalia Terenti, Gavril-Ionel Giurgi, Lorant Szolga, Ioan Stroia, Anamaria Terec, Ion Grosu, Andreea Petronela Crișan
Publikováno v:
Molecules, Vol 27, Iss 4, p 1229 (2022)
Four acceptor–donor–acceptor (A–D–A)-type molecules bearing indacenodithiophene as donating central core and various end-capping acceptor units have been designed and synthesised as n-type materials suitable for organic solar cells (OSCs). Th
Externí odkaz:
https://doaj.org/article/2e52bc63b7ed461cb0d5588b7190c631
Autor:
Claudia Lar, Adrian Woiczechowski-Pop, Attila Bende, Ioana Georgeta Grosu, Natalia Miklášová, Elena Bogdan, Niculina Daniela Hădade, Anamaria Terec, Ion Grosu
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 1370-1377 (2018)
The aromatic nucleophilic substitution reaction based synthesis of a three-armed cryptand displaying 2,4,6-triphenyl-1,3,5-triazine units as caps and pyridine rings in the bridges, along with NMR, MS and molecular modelling-based structural analysis
Externí odkaz:
https://doaj.org/article/e161c863e6d2499081f6a5e4584e2a95
Autor:
Andreea Petronela Diac, Ana-Maria Ţepeş, Albert Soran, Ion Grosu, Anamaria Terec, Jean Roncali, Elena Bogdan
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 12, Iss 1, Pp 825-834 (2016)
New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significa
Externí odkaz:
https://doaj.org/article/e4f3b684b1754da29a2ee657eb3067f7
Autor:
Cosmin Vasile Crişan, Albert Soran, Attila Bende, Niculina Daniela Hӑdade, Anamaria Terec, Ion Grosu
Publikováno v:
Molecules, Vol 25, Iss 17, p 3789 (2020)
The high-yield synthesis and the structural investigation of a new cryptand with C3 symmetry, exhibiting 2,4,6-triphenyl-1,3,5-triazine central units and pyridine-based bridges, are reported. The structure of the compound was investigated by single c
Externí odkaz:
https://doaj.org/article/6053fb0ee0b642c4bb82349c4ac4ecf1
Publikováno v:
Molecules, Vol 13, Iss 11, Pp 2848-2858 (2008)
The configurational and conformational behavior of some new 3,3,9,9-tetrasubstituted-2,4,8,10-tetraoxaspiro[5.5]undecane derivatives with axial chirality was investigated by conformational analysis and variable temperature NMR experiments.
Externí odkaz:
https://doaj.org/article/457825cec94543b69dd51828b4f30fa9
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 2, Pp o310-o311 (2012)
The title compound, C21H17ClO3, which crystallizes as one of two possible oxo/hydroxy-fulvene prototropic tautomers, possesses a strong intramolecular O—H...O hydrogen bond that closes a seven-membered ring. The dihedral angles between the central
Externí odkaz:
https://doaj.org/article/6efb162110a64a4694a3182221bd9bea