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1.  (2-{[4-(Chlorido­mercur­yl)phen­yl]imino­meth­yl}pyridine-κ2 N,N′)di­iodido­mercury(II) dimethyl sulfoxide monosolvate 
The title dimethyl sulfoxide solvate, [Hg2(C12H9ClN2)I2]·C2H6OS, features tetra­hedrally and linearly coordinated HgII atoms. The distorted tetrahedral coordination sphere is defined by chelating N atoms that define an acute angle [69.6 (3)°] and two I atoms that form a wide angle [142.80 (4)°]. The linearly coordinated HgII atom [177.0 (4)°] exists with a donor set defined by C and Cl atoms. Secondary inter­actions are apparent in the crystal packing with the tetra­hedrally and linearly coordinated HgII atoms expanding their coordination environments by forming weak Hg⋯I [3.772 (7) Å] and Hg⋯O [2.921 (12) Å] inter­actions, respectively. Mercury-containing mol­ecules stack along the a axis, are connected by π–π inter­actions [inter-centroid distance between pyridine and benzene rings = 3.772 (7) Å] and define channels in which the dimethyl sulfoxide mol­ecules reside. The latter are connected by the aforementioned Hg⋯O inter­actions as well as C—H⋯I and C—H⋯O inter­actions, resulting in a three-dimensional architecture.
doi:10.1107/S1600536813029693
PMCID: PMC3884979  PMID: 24454154
2.  Di-μ-iodido-bis­(iodido­{methyl 4-[(pyridin-2-yl­methyl­idene)amino]­benzoate-κ2 N,N′}cadmium) 
The complete binuclear molecule of the title compound, [Cd2I4(C14H12N2O2)2], is generated by the application of a centre of inversion. The Cd—I bond lengths of the central core are close and uniformly longer than the exocyclic Cd—I bond. The coordination sphere of the CdII atom is completed by two N atoms of a chelating methyl 4-[(pyridin-2-yl­methyl­idene)amino]­benzoate ligand, and is based on a square pyramid with the terminal I atom in the apical position. The three-dimensional crystal packing is stabilized by C—H⋯O and C—H⋯π inter­actions, each involving the pyridine ring.
doi:10.1107/S160053681302905X
PMCID: PMC3884272  PMID: 24454048
3.  Bis{2-[(E)-(5-tert-butyl-2-hy­droxy­phen­yl)diazen­yl]benzoato}dimethyl­tin(IV) 
In the title diorganotin dicarboxyl­ate, [Sn(CH3)2(C17H17N2O3)2], the tin(IV) atom is six-coordinated by four O atoms derived from asymmetrically coordinating carboxyl­ate ligands, and two methyl-C atoms. The resulting C2O4 donor set defines a skew-trapezoidal bipyramid with the Sn—C bonds disposed over the weaker Sn—O bonds. Within each carboxyl­ate ligand, the hydroxyl-H atom forms bifurcated O—H⋯(O,N) hydrogen bonds with carboxyl­ate-O and azo-N atoms. The dihedral angles between the benzene rings in the two ligands are 10.44 (11) and 34.24 (11)°. In the crystal, centrosymmetric dimers are formed through pairs of Sn⋯O inter­actions [2.8802 (16) Å], and the dimers are linked into supra­molecular layers in the ac plane by C—H⋯π inter­actions.
doi:10.1107/S1600536811036543
PMCID: PMC3201396  PMID: 22065466
4.  Tetra­kis(μ2-4-amino­benzoato)di-μ3-oxido-tetra­kis[dibutyl­tin(IV)] 
The mol­ecule of the title compound, [Sn4(C4H9)8(C7H6NO2)4O2], lies about an inversion centre and is a tetra­nuclear bis­(tetra­butyl­dicarboxyl­ato­distannoxane) complex containing a planar Sn4O2 core in which two μ3-oxide O atoms connect an Sn2O2 ring to two exocyclic Sn atoms. Each Sn atom has a highly distorted octa­hedral coordination. In the mol­ecule, the carboxyl­ate groups of two amino­benzoate ligands bridge the central and exocyclic Sn atoms, while two further amino­benzoate ligands have highly asymmetric bidentate chelation to the exocyclic Sn atoms plus long O⋯Sn inter­actions with the central Sn atoms. Each Sn atom is also coordinated by two pendant n-butyl ligands, which extend roughly perpendicular to the plane of the Sn4O10 core. Only one of the four unique hydrogen-bond donor sites is involved in a classic N—H⋯O hydrogen bond, and the resulting supra­molecular hydrogen-bonded structure is an extended two-dimensional network which lies parallel to the (100) plane and consists of a checkerboard pattern of four-connected mol­ecular cores acting as nodes. The amine groups not involved in the hydrogen-bonding inter­actions have significant N—H⋯π inter­actions with neighbouring amino­benzene rings.
doi:10.1107/S0108270110003033
PMCID: PMC2855585  PMID: 20203395
5.  4-[(E)-(5-tert-Butyl-2-hydroxy­phen­yl)diazen­yl]benzoic acid benzene hemisolvate 
The title benzene hemisolvate, C17H18N2O3·0.5C6H6, features an essentially planar (the r.m.s. deviation of the non-H atoms, excluding methyl-C, is 0.071 Å) diazo mol­ecule with an E conformation about the N=N bond, and a half-mol­ecule of benzene disposed about a centre of inversion. The dihedral angle formed between the benzene rings of the diazo mol­ecule is 7.69 (12)°. In the crystal, centrosymmetrically related dimers associate via the eight-membered carboxylic acid dimer synthon, {⋯HOC(=O)}2, and these are connected into a supra­molecular chain along the b axis via C—H⋯O contacts.
doi:10.1107/S1600536810003880
PMCID: PMC2983727  PMID: 21580311
6.  An ortho­rhom­bic polymorph of 5-[(4-methyl­phen­yl)diazen­yl]salicylaldehyde 
The title compound, C14H12N2O2, is an ortho­rhom­bic polymorph of the previously reported monoclinic form [Bakir et al. (2005 ▶). Acta Cryst. E61, o1611–o1613]. The dihedral angle between the aromatic rings is 4.32 (13)°. The mol­ecular structures of the two polymorphs, including short intra­molecular O—H⋯O hydrogen bonds between the the hydr­oxy and keto groups, are quite similar but their crystal packings are distinct. Unlike the monoclinic form, in which centrosymmetrically related hydr­oxy and keto groups form {⋯H⋯O}2 synthons via weak O—H⋯O contacts, leading to dimeric aggregates, in the ortho­rhom­bic form, the hydrogen bonding between these groups leads to the formation of supra­molecular chains orientated along the a axis.
doi:10.1107/S1600536809046868
PMCID: PMC2971774  PMID: 21578791
7.  2-[(E)-(5-tert-Butyl-2-hydroxy­phen­yl)­diazen­yl]benzoic acid 
The title compound, C17H18N2O3, is approximately planar, owing in part to an intra­molecular bifurcated O—H⋯(N,O) hydrogen bond; the dihedral angle between the two aromatic rings is 23.86 (9)°. In the crystal struture, centrosymmetrically related mol­ecules associate into dimers via the eight-membered carboxyl­ate {⋯H—O—C=O}2 synthon.
doi:10.1107/S160053680803290X
PMCID: PMC2959775  PMID: 21580987

Results 1-7 (7)