scholarly journals {μ-2-[(3-Amino-2,2-dimethylpropyl)iminomethyl]-6-methoxyphenolato-1:2κ5O1,O6:N,N′,O1}{2-[(3-amino-2,2-dimethylpropyl)iminomethyl]-6-methoxyphenolato-1κ3N,N′,O1}-μ-azido-1:2κ2N:N-azido-2κN-methanol-2κO-dinickel(II)

2012 ◽  
Vol 68 (8) ◽  
pp. m1027-m1028
Author(s):  
Akbar Ghaemi ◽  
Saeed Rayati ◽  
Kazem Fayyazi ◽  
Seik Weng Ng ◽  
Edward R. T. Tiekink

Two distinct coordination geometries are found in the binuclear title complex, [Ni2(C13H19N2O2)2(N3)2(CH3OH)], as one Schiff base ligand is pentadentate, coordinatingviathe anticipated oxide O, imine N and amine N atoms (as for the second, tridentate, ligand) but the oxide O is bridging and coordination also occurs through the methoxy O atom. The NiIIatoms are linked by a μ2-oxide atom and one end of a μ2-azide ligand, forming an Ni2ON core. The coordination geometry for the NiIIatom coordinated by the tridentate ligand is completed by the methoxy O atom derived from the pentadentate ligand, with the resulting N3O3donor set defining afacoctahedron. The second NiIIatom has itscis-octahedral N4O2coordination geometry completed by the imine N and amine N atoms of the pentadentate Schiff base ligand, a terminally coordinated azide N and a methanol O atom. The arrangement is stabilized by an intramolecular hydrogen bond between the methanol H and the oxide O atom. Linear supramolecular chains along theaaxis are formed in the crystal packing whereby two amine H atoms from different amine atoms hydrogen bond to the terminal N atom of the monodentate azide ligand.

2006 ◽  
Vol 62 (7) ◽  
pp. m1548-m1549
Author(s):  
Xing-You Xu ◽  
Tong-Tao Xu ◽  
Shuai-Shuai Ni ◽  
Jian Gao ◽  
Da-Qi Wang

The title complex, [ZnCl2(C16H17NO2)2], displays a distorted tetrahedral coordination geometry around the ZnII ion. The Schiff base inner salt, (benzylimino)ethyl-5-methoxyphenol, coordinates in a monodentate manner to the ZnII ion via the deprotonated hydroxy groups. The protonated imino groups form intramolecular hydrogen bonds with the deprotonated hydroxyl groups of the same Schiff base ligand.


2012 ◽  
Vol 68 (8) ◽  
pp. m1033-m1034
Author(s):  
Reza Takjoo ◽  
Seik Weng Ng ◽  
Edward R. T. Tiekink

The VIVatom in the title complex, [V(C19H17N3O2S)O], is coordinated by two N and two O atoms of the dianionic tetradentate Schiff base ligand and the terminal oxide O atom. The N2O3donor set defines a square-pyramidal coordination geometry with the oxide O atom in the apical site. Some buckling in the tetradentate ligand is indicated by the dihedral angle of 17.92 (19)° between the six-membered chelate rings. Supramolecular chains are formed along thebaxisviaC—H...O contacts in the crystal. The chains are connected into a layer in theabplaneviaC—H...π interactions. The atoms comprising the –SCH2—CH=CH2and methyl substituents were found to be disordered in a 0.916 (2):0.088 (2) ratio. The crystal studied was found to be twinned by nonmerohedry with a 28.1 (4)% minor twin component.


IUCrData ◽  
2016 ◽  
Vol 1 (9) ◽  
Author(s):  
Liang Chen ◽  
Xuebin Deng

The mononuclear TiIVtitle complex, [Ti(C28H22N2O2)(C3H7O)2]·0.5C6H14, crystallizes as ann-hexane hemisolvate. The TiIVatom is coordinated by a dianionic tetradentate biphenyl Schiff base ligand and two O atoms of two propan-2-olate anions in a distorted TiN2O4octahedral coordination geometry, in which the two N atoms are in acisconfiguration. In the crystal, complex molecules are stacked parallel to [100], leaving space for channels parallel to [001] where the solvent molecules are located.


2007 ◽  
Vol 63 (3) ◽  
pp. o1407-o1408
Author(s):  
Yun-Fa Zheng ◽  
Liang-Gui Wang ◽  
Guo-Bing Yan

The title compound, C18H11F4NO, a Schiff base, has been structurally characterized. One intramolecular hydrogen bond influences the conformation of the molecule. The crystal structure is extended into a one-dimensional chain along the c axis via π–π stacking interactions.


2007 ◽  
Vol 63 (11) ◽  
pp. o4308-o4309 ◽  
Author(s):  
Ray J. Butcher ◽  
Jerry P. Jasinski ◽  
Anil N. Mayekar ◽  
B. Narayana ◽  
H. S. Yathirajan

In the title compound, C17H12Br3Cl2NO, the mean planes of the 3,5-dibromo-4-phenyl and 2,4-dichlorophenyl groups make a dihedral angle of 72.4 (2)°. The dihedral angles between the 2-bromoprop-2-en-1-one group and the two phenyl ring groups (3,5-dibromo-4-phenyl and 2,4-dichlorophenyl) are 71.1 (1) and 10.9 (4)°, respectively. The crystal packing is stabilized by intermolecular N—H...O hydrogen-bond interactions between the ethylamino H atom and the propyl ketone O atom, with the 3,5-dibromo-4-phenyl rings linked in chains in an alternate inverted pattern parallel and oblique to the ac face and diagonally along the a axis of the unit cell. An intramolecular hydrogen bond between the ethyl amino H atom and the 5-Br atom from the 3,5-dibromo-4-phenyl group helps stabilize the molecular conformation.


2006 ◽  
Vol 62 (4) ◽  
pp. m849-m850 ◽  
Author(s):  
Xiao-Yang Qiu

The title compound, [Cu(C17H21N2O)(N3)], is a mononuclear copper(II) complex. The central CuII ion is four-coordinated by one O and two N atoms of the Schiff base ligand, and by one N atom of an azide anion, forming a distorted square-planar coordination geometry.


2014 ◽  
Vol 70 (9) ◽  
pp. 121-123
Author(s):  
Matthias Zeller ◽  
Jonas Warneke ◽  
Vladimir Azov

The structure of the title compound, C14H15ClN2O4, prepared by reaction of a methacryloyl dimer with nitroaniline, was determined to establish the relative substituent orientation on the cyclopentanone ring. In agreement with an earlier proposed reaction mechanism, the amide group and the methyl group adjacent to the chloro substituent adopt equatorial positions and relativecisorientation, whereas the Cl substituent itself and the methyl group adjacent to the amide have axial orientations relative to the mean plane of the five-membered ring. The conformation of the molecule is stabilized by one classical N—H...O (2.18 Å) and one non-classical C—H...O (2.23 Å) hydrogen bond, each possessing anS(6) graph-set motif. The crystal packing is defined by several non-classical intramolecular hydrogen bonds, as well as by partial stacking of the aromatic rings.


2012 ◽  
Vol 68 (4) ◽  
pp. m517-m517
Author(s):  
Yi-Fang Deng ◽  
Xue Nie ◽  
Chun-Hua Zhang

In the title compound, [Zn(C8H6ClNO4S)(C10H8N2)(H2O)], the ZnIIatom is six-coordinated by two O atoms and one N atom from a tridentate Schiff base ligand and two N atoms from a chelating 2,2′-bipyridine ligand and one water molecule, forming a slightly distorted octahedral geometry. In the crystal, O—H...O hydrogen bonds link pairs of complex molecules into dimers. An intramolecular O—H...O hydrogen bond is also present.


2007 ◽  
Vol 63 (11) ◽  
pp. m2812-m2812 ◽  
Author(s):  
Lai-Jin Tian ◽  
Hong-Jun Yang ◽  
Zhong-Hai Ni

The title compound, [Ni(C23H17N4O)(N3)], was obtained by the reaction of the Schiff base ligand 2-[(tri-2-pyridylmethyl)iminomethyl]phenol with sodium azide and nickel(II) perchlorate in methanol solution. The NiII atom is four-coordinated by the phenolate O, the imine N and a pyridine N atom of the Schiff base ligand, and by the terminal N atom of an azide ligand, forming a square-planar geometry. The other two pyridyl rings are oriented at an angle of 72.29 (11)° to each other.


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