Search results for "4-D"
showing 10 items of 955 documents
Intramolecular Hydrogen Bond, Hirshfeld Analysis, AIM; DFT Studies of Pyran-2,4-dione Derivatives
2021
Intra and intermolecular interactions found in the developed crystals of the synthesized py-ron-2,4-dione derivatives play crucial rules in the molecular conformations and crystal stabili-ties, respectively. In this regard, Hirshfeld calculations were used to quantitatively analyze the different intermolecular interactions in the crystal structures of some functionalized py-ran-2,4-dione derivatives. The X-ray structure of pyran-2,4-dione derivative namely (3E,3′E)-3,3′-((ethane-1,2-diylbis(azanediyl))bis(phenylmethanylylidene))bis(6-phenyl-2H-pyran-2,4(3H)-dione) was determined. It crystallized in the monoclinic crystal system and C2/c space group with unit cell parameters: a = 14.0869(4) …
CCDC 1576743: Experimental Crystal Structure Determination
2019
Related Article: Arkalekha Mandal, Kari Rissanen, Prasenjit Mal|2019|CrystEngComm|21|4401|doi:10.1039/C9CE00561G
Poly[[tetramethanolbis[4-oxo-3-(pyridin-4-yl)-1-(2,4,6-trichlorophenyl)-4,5-dihydro-1H-pyrazolo[3,4-d]pyrimidin-6-olato]disodium]–diethyl ether–metha…
2016
In the title compound, [Na2(C16H7Cl3N5O2)2(CH3OH)4]·C4H10O·2CH3OH, the central pyrazolo[3,4-d]pyrimidine system makes dihedral angles of 82.98 (7)° with the trichlorophenyl ring and 13.11 (15)° with the pyridine ring. The sodium ion has an octahedral environment, being coordinated by four methanol molecules and one O and one N atom of two different heterocyclic ring systems.
Redox reaction between amino‐(3,4‐dihydroxyphenyl)methyl phosphonic acid and dopaquinone is responsible for the apparent inhibitory effect on tyrosin…
2002
Amino‐(3,4‐dihydroxyphenyl)methyl phosphonic acid, the phosphonic analog of 3,4‐dihydroxyphenylglycine, had been previously reported as a potent inhibitor of tyrosinase. The mechanism of the apparent enzyme inhibition by this compound has now been established. Amino‐(3,4‐dihydroxyphenyl)methyl phosphonic acid turned out to be a substrate and was oxidized to o‐quinone, which evolved to a final product identified as 3,4‐dihydroxybenzaldehyde, the same as for 3,4‐dihydroxyphenylglycine. Monohydroxylated compounds (amino‐(3‐hydroxyphenyl)methyl phosphonic acid and amino‐(4‐hydroxyphenyl)methyl phosphonic acid) were not oxidized, neither was 4‐hydroxy‐l‐phenylglycine. However, the relatively hig…
CCDC 1444032: Experimental Crystal Structure Determination
2016
Related Article: Fares Ibrahim Amr, Carlos Vila, Gonzalo Blay, M. Carmen Muñoz and José R. Pedro|2016|Adv.Synth.Catal.|358|1583|doi:10.1002/adsc.201600036
CCDC 953879: Experimental Crystal Structure Determination
2013
Related Article: Huayan Yang, Yu Wang, Huaqi Huang, Lars Gell, Lauri Lehtovaara, Sami Malola, Hannu Hakkinen, Nanfeng Zheng|2013|Nat.Commun.|4|2422|doi:10.1038/ncomms3422
CCDC 1979322: Experimental Crystal Structure Determination
2020
Related Article: Noelia Maldonado, Josefina Perles, José Ignacio Martínez, Carlos J. Gómez-García, María-Luisa Marcos, Pilar Amo-Ochoa|2020|Cryst.Growth Des.|20|5097|doi:10.1021/acs.cgd.0c00268
CCDC 169925: Experimental Crystal Structure Determination
2001
Related Article: B.Abouhamza, M.Ait Ali, S.Allaoud, O.Blacque, B.Frange, A.Karim|2001|Acta Crystallogr.,Sect.C:Cryst.Struct.Commun.|57|796|doi:10.1107/S0108270101006187
CCDC 781063: Experimental Crystal Structure Determination
2010
Related Article: I.Bergner, C.Wiebe, N.Meyer, T.Opatz|2009|J.Org.Chem.|74|8243|doi:10.1021/jo901759u
CCDC 751051: Experimental Crystal Structure Determination
2010
Related Article: J.Vicente, I.Saura-Llamas, J.Turpin, D.Bautista, C.R.de Arellano, P.G.Jones|2009|Organometallics|28|4175|doi:10.1021/om9002895