Zobrazeno 1 - 10
of 37
pro vyhledávání: '"Cristina Geiger"'
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 75, Iss 2, Pp 272-276 (2019)
Hydrogen bonding plays an important role in the design of solid-state structures and gels with desirable properties. 1-(4-Hydroxybenzyl)-2-(4-hydroxyphenyl)-5,6-dimethyl-1H-benzimidazole was isolated as the acetone disolvate, C22H20N2O2·2C3H6O. O—
Externí odkaz:
https://doaj.org/article/18bbf83381004306ad91346b9989f64c
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 5, Pp 594-599 (2018)
An understanding of the driving forces resulting in crystallization vs organogel formation is essential to the development of modern soft materials. In the molecular structure of the title compound, methyl 10-[4-(4-hydroxyphenyl)phenoxy]decanoate (MB
Externí odkaz:
https://doaj.org/article/81cbb27009be426db1d1f63b61201ab3
Autor:
H. Cristina Geiger, David K. Geiger, William R. Roberts, Dominic L. Morell, Paul Huttunen, Jennifer L. Schulman, Melanie Tran, Dori Farthing
Publikováno v:
Gels, Vol 4, Iss 2, p 34 (2018)
Because the factors favoring the formation of well-formed single crystals are dissimilar to those conducive to gel formation, few examples of single-crystal structural characterizations of organogelators are found in the literature. A series of biphe
Externí odkaz:
https://doaj.org/article/408becde789e4417abeb15a1b084277c
Publikováno v:
Acta Crystallographica Section E, Vol 70, Iss 4, Pp o486-o487 (2014)
The title compound, C18H13Br3N2S2, was obtained via the reaction of N-bromosuccinamide with 5,6-dimethyl-2-(thiophen-2-yl)-1-[(thiophen-2-yl)methyl]-1H-benzimidazole. The compound exhibits rotational disorder of the 5-bromothiophen-2-yl substituent w
Externí odkaz:
https://doaj.org/article/89b07ed61bb84527bc83bb50bcec26cc
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 6, Pp o916-o916 (2013)
The asymmetric unit of the title compound, C10H8N2S2, is composed of two independent half-molecules, each residing on a center of symmetry. In the crystal, weak C—H...π interactions join the two symmetry-independent molecules together into interli
Externí odkaz:
https://doaj.org/article/5fa06ede621f4b31a22b6530668195a9
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 10, Pp o3006-o3007 (2012)
The title hydrated salt, C21H17N2O3+·Cl−·H2O, exhibits disorder in one of the furan rings. The major and minor components have a refined occupancy ratio of 0.844 (19):0.156 (19). The structure displays intermolecular hydrogen bonding involving th
Externí odkaz:
https://doaj.org/article/57523c6b43e9485a94858e9341efc9d1
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 10, Pp o2867-o2867 (2012)
In the title molecule, C11H9N3O2S, the thiophene and benzene rings form a dihedral angle of 17.68 (9)°. The thiophene S atom and the imine N atom are syn with respect to each other. In the crystal, N—H...O and N—H...N hydrogen bonds connect mole
Externí odkaz:
https://doaj.org/article/2ef0f672eba247d491bd3a95616aab00
Publikováno v:
Acta Crystallographica Section E, Vol 68, Iss 2, Pp o420-o420 (2012)
In the title compound, C16H12N2S2, the thiophene groups are rotationally disordered over two sets of sites, by approximately 180°, with occupancy ratios of 0.916 (2):0.084 (2) and 0.903 (2):0.097 (2). The major components of the thiophene and methyl
Externí odkaz:
https://doaj.org/article/2aa5cef4461a4a82b1a8a3919a54c371
Autor:
David K. Geiger, Paul Huttunen, H. Cristina Geiger, Jennifer L Schulman, Dominic L Morell, Dori Farthing, Melanie Tran, William R. Roberts
Publikováno v:
Gels; Volume 4; Issue 2; Pages: 34
Gels
Gels, Vol 4, Iss 2, p 34 (2018)
Gels
Gels, Vol 4, Iss 2, p 34 (2018)
Because the factors favoring the formation of well-formed single crystals are dissimilar to those conducive to gel formation, few examples of single-crystal structural characterizations of organogelators are found in the literature. A series of biphe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7cd13071721448bf02bd18713feb3bb8
https://pubmed.ncbi.nlm.nih.gov/30674810
https://pubmed.ncbi.nlm.nih.gov/30674810
Publikováno v:
Acta crystallographica. Section C, Structural chemistry. 73(Pt 10)
There are few examples of single-crystal structure determinations of gelators, as gel formation requires that the dissolved gelator self-assemble into a three-dimensional network structure incorporating solvent via noncovalent interactions rather tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2d2a679c3cc9fcd0ac2372e3cc3bb018
https://pubmed.ncbi.nlm.nih.gov/28978785
https://pubmed.ncbi.nlm.nih.gov/28978785