共查询到20条相似文献,搜索用时 15 毫秒
1.
Masashi Kawai Hidetaka Yuge Takeshi Ken Miyamoto 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(12):m581-m582
The title diphenylcarbene porphyrin complex (diphenylcarbenyl‐κC)(methanol‐κO)(5,10,15,20‐tetra‐p‐tolylporphyrinato‐κ4N)ruthenium(II) methanol solvate, [Ru(C13H10)(C48H36N4)(CH4O)]·CH4O, has a six‐coordinate Ru atom with a methanol molecule as the second axial ligand. The carbene fragment is slightly distorted from an ideal sp2 configuration, with a C(phenyl)—C(carbene)—C(phenyl) angle of 112.2 (3)°. The Ru—C bond length of 1.845 (3) Å is comparable with other carbene complexes. The two phenyl rings of the carbene ligand are perpendicular to the carbene plane. Methanol solvate molecules link the methanol ligands of adjacent porphyrin complexes via hydrogen bonds. 相似文献
2.
Hidetaka Yuge Takeshi Ken Miyamoto Tomofumi Kikuchi Yukihiro Iwasaki 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(12):m594-m596
In the first bis[ruthenium(II)–porphyrin]–dicarbene complex, μ‐[1,4‐phenylenebis(phenylmethylidene‐κC)]bis[(ethanol‐κO)(5,10,15,20‐tetra‐p‐tolylporphyrinato‐κ4N)ruthenium(II)] 1,2‐dichloroethane trisolvate, [Ru2(C20H14)(C48H36N4)2(C2H6O)2]·3C2H4Cl2, an inversion center is located at the center of the μ‐phenylene group, leading to a parallel arrangement for the pair of porphyrin ring systems. The bond lengths and angles compare favourably with literature values for ruthenium–porphyrin–monocarbene complexes; the Ru=C(carbene) bond length and the C(phenyl)—C(carbene)—C(phenylene) angle are 1.865 (3) Å and 112.3 (3)°, respectively. The RuII ion is displaced out of the C20N4 porphyrin least‐squares plane (by 0.2373 Å) toward the bridging ligand of the Ci‐symmetry dimer. The porphyrin ring systems of the dimer thus exhibit mildly domed conformations. 相似文献
3.
Satoko Wada Hidetaka Yuge Takeshi Ken Miyamoto 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(9):m369-m370
The stable title trifluoromethyl‐substituted carbenyl metalloporphyrin, [Ru(C15H8F6)(C48H36N4)], has a five‐coordinate Ru atom which is displaced from the porphyrin N4 plane towards the axial carbene ligand by 0.230 (3) Å. The Ru—C(carbene) bond coincides with a crystallographic twofold axis and its length of 1.841 (6) Å is notably shorter than the value of 1.868 (3) Å in the pyridine adduct. 相似文献
4.
Eric P. Kelson Proma P. Phengsy Atta M. Arif 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(5):517-519
The aldehyde moiety in the title complex, chloro(2‐pyridinecarboxaldehyde‐N,O)(2,2′:6′,2′′‐terpyridine‐κ3N)ruthenium(II)–chloro(2‐pyridinecarboxylic acid‐N,O)(2,2′:6′,2′′‐terpyridine‐κ3N)ruthenium(II)–perchlorate–chloroform–water (1.8/0.2/2/1/1), [RuCl(C6H5NO)(C15H11N3)]1.8[RuCl(C6H5NO2)(C15H11N3)]0.2(ClO4)2·CHCl3·H2O, is a structural model of substrate coordination to a transfer hydrogenation catalyst. The title complex features two independent RuII complex cations that display very similar distorted octahedral coordination provided by the three N atoms of the 2,2′:6′,2′′‐terpyridine ligand, the N and O atoms of the 2‐pyridinecarboxaldehyde (pyCHO) ligand and a chloride ligand. One of the cation sites is disordered such that the aldehyde group is replaced by a 20 (1)% contribution from a carboxylic acid group (aldehyde H replaced by carboxyl O—H). Notable dimensions in the non‐disordered complex cation are Ru—N 2.034 (2) Å and Ru—O 2.079 (2) Å to the pyCHO ligand and O—C 1.239 (4) Å for the pyCHO carbonyl group. 相似文献
5.
Kai Hirasawa Hidetaka Yuge Takeshi Ken Miyamoto 《Acta Crystallographica. Section C, Structural Chemistry》2008,64(2):m97-m100
The chiral metalloporphyrin (dibenzoylmethylene‐κC)(ethanol‐κO){5,10,15,20‐tetrakis[(1S,4R,5R,8S)‐1,2,3,4,5,6,7,8‐octahydro‐1,4:5,8‐dimethanoanthracen‐9‐yl]porphyrinato‐κ4N}ruthenium(II)–ethanol–dichloromethane (1/2/2), [Ru(C84H76N4)(C15H10O2)(C2H6O)]·2C2H6O·2CH2Cl2, and its enantiomorph were prepared from enantiomerically pure porphyrins. The enantiomers are potential versatile catalysts for asymmetric cyclopropanation, aziridination or epoxidation. In each compound, the rather large dibenzoylcarbene group is squeezed between four columnar 1,2,3,4,5,6,7,8‐octahydro‐1,4:5,8‐dimethanoanthracen‐9‐yl groups at the meso positions resulting in a doming deformation of the porphyrin core. The dibenzoylcarbene group has an anti conformation. The benzoyl O atoms make short van der Waals contacts (< 2.6 Å) with the methine groups of the chiral columnar substituents at the 10 and 20 positions of the porphyrin rings. A hydrogen‐bonded supramolecular chain is formed parallel to the b axis by interactions between the benzoyl O atom and the hydroxy groups of the coordinated and uncoordinated ethanol molecules. 相似文献
6.
G. Von Poelhsitz B. L. Rodrigues A. A. Batista 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(9):m424-m427
The crystal structures of [1,3‐bis(diphenylphosphino)ethane‐κ2P,P′](pyridine‐2‐sulfinato‐κ2N,S)(pyridine‐2‐thiolato‐κ2N,S)ruthenium(II), [Ru(C5H4NO2S)0.33(C5H4NS)1.67(C26H24P2)] or [Ru(pySO2)1−x(pyS)1+x(dppe)] (x = 0.67), (I), and [1,3‐bis(diphenylphosphino)propane‐κ2P,P′](pyridine‐2‐sulfinato‐κ2N,S)(pyridine‐2‐thiolato‐κ2N,S)ruthenium(II), [Ru(C5H4NO2S)0.355(C5H4NS)1.645(C27H26P2)] or [Ru(pySO2)1−x(pyS)1+x(dppp)] (x = 0.645), (II), are composed of neutral distorted octahedral RuII complexes with chelating pyridine‐2‐thiolate, pyridine‐2‐sulfinate and biphosphine ligands. The S atoms are trans to each other, while pairs of P and N atoms are in cis positions. Partial double‐bond character is observed for C—S. The crystal packing consists of monolayers stabilized by C—H⋯O and C—H⋯S interactions, and is affected by the alkyl‐chain lengths. 相似文献
7.
Yael Diskin‐Posner Goutam Kumar Patra Israel Goldberg 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(6):m344-m346
The title compound, [5,10,15,20‐meso‐tetrakis(4‐hydroxyphenyl)porphyrinato‐κ4N]zinc(II) tris(dibenzo‐24‐crown‐8) methanol tetrasolvate, [Zn(C44H28N4O4)]·3C24H32O8·4CH4O, was synthesized and its molecular structure precisely characterized by low‐temperature single‐crystal analysis. All the components are involved in hydrogen bonding with each other, thus forming an extensively hydrogen‐bonded supramolecular lattice. The functionalized porphyrin moiety coordinates both equatorially and axially to the neighboring species. 相似文献
8.
Brian W. Skelton A. Fiona Waters Claire R. Whitaker Allan H. White 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(11):m435-m438
Both of the title compounds, catena‐poly[[[tetraaquamagnesium(I)]‐μ‐4,4′‐bipyridine‐κ2N:N′] diiodide bis(4,4′‐bipyridine) solvate], {[Mg(C10H8N2)(H2O)4]I2·2C10H8N2}n, (I), and catena‐poly[[[μ‐4,4′‐bipyridine‐bis[diiodobis(propan‐1‐ol)strontium(I)]]‐di‐μ‐4,4′‐bipyridine‐κ4N:N′] bis(4,4′‐bipyridine) solvate], {[Sr2I4(C10H8N2)3(C3H8O)4]·2C10H8N2}n, (II), are one‐dimensional polymers which are single‐ and double‐stranded, respectively, the metal atoms being linked by the 4,4′‐bipyridine moieties. The Mg complex, (I), is [cis‐{(H2O)4Mg(N‐4,4′‐bipyridine‐N′)(2/2)}](∞|∞)I2·4,4′‐bipyridine and Mg has a six‐coordinate quasi‐octahedral coordination environment. The Sr complex, (II), is isomorphous with its previously defined Ba counterpart [Kepert, Waters & White (1996). Aust. J. Chem. 49 , 117–135], being [(propan‐1‐ol)2I2Sr(N‐4,4′‐bipyridine‐N′)(3/2)](∞|∞)·4,4′‐bipyridine, with the I atoms trans‐axial in a seven‐coordinate pentagonal–bipyramidal Sr environment. 相似文献
9.
Kanidtha Hansongnern Uraiwan Saeteaw Jack Cheng Fen‐Ling Liao Tian‐Huey Lu 《Acta Crystallographica. Section C, Structural Chemistry》2001,57(8):895-896
The Ru—N bond distances in the title complex, [Ru(NO2)(C11H9N3)(C15H11N3)]BF4 or [Ru(NO2)(tpy)(azpy)]BF4, [tpy is 2,2′:6′,2′′‐terpyridine and azpy is 2‐(phenylazo)pyridine], are Ru—Npy 2.063 (4), Ru—Nazo 2.036 (4), Ru—Nnitro 2.066 (3) Å, and Ru—Ntpy 2.082 (4), 1.982 (3) and 2.074 (4) Å. The azo N atom is trans to the nitro group. The azo N=N bond length is 1.265 (5) Å, which is the shortest found in such complexes to date. This indicates a multiple bond between Ru and the N atom of the nitro group, and π‐backbonding [dπ(Ru) π*(azo)] is decreased. 相似文献
10.
Xiue Lin Yan‐Qin Wang Rong Cao Feng Li Wen‐Hua Bi 《Acta Crystallographica. Section C, Structural Chemistry》2005,61(6):m292-m294
The title cadmium(II) polymer, catena‐poly[[[bis(4‐aminopyridine‐κN)aquacadmium(II)]‐μ‐1,4‐phenylenediacetato‐κ4O,O′:O′′,O′′′] dihydrate], {[Cd(C10H8O4)(C5H6N2)2(H2O)]·2H2O}n, comprises one‐dimensional wave‐like chains, in which the Cd atom is coordinated by 1,4‐phenylenediacetate and 4‐aminopyridine molecules. The 1,4‐phenylenediacetate ligands lie about inversion centres. Extensive hydrogen‐bonding interactions between the chains lead to a three‐dimensional structure. Free water molecules form chains in the structure. 相似文献
11.
Tamami Koshiyama Masako Kato 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(11):m446-m449
The title PtII complexes, viz. (2,2′‐bipyridine‐κ2N,N′)[(1R,2R)‐1,2‐diaminocyclohexane‐κ2N,N′]platinum(II) bis(hexafluorophosphate), [Pt(C6H14N2)(C10H8N2)](PF6)2, and [(1R,2R)‐1,2‐diaminocyclohexane‐κ2N,N′](1,10‐phenanthroline‐κ2N,N′)platinum(II) bis(hexafluorophosphate), [Pt(C6H14N2)(C12H8N2)](PF6)2, containing an aromatic α‐diimine and a non‐planar diaminocyclohexane, both form a ladder‐type structure, which is constructed via loose π–π stacking on the α‐diimine ligands and hydrogen bonding between the cyclic amines and the counter‐anions. In the former compound, there are two independent complex cations, both of which have a twofold axis through the Pt atom. 相似文献
12.
Sankar Muniappan Sophia Liptsman Israel Goldberg 《Acta Crystallographica. Section C, Structural Chemistry》2006,62(4):m140-m143
Tetrakis(4‐methoxycarbonylphenyl)porphyrin, or tetramethyl 4,4′,4′′,4′′′‐porphyrin‐5,10,15,20‐tetrabenzoate, crystallizes as a nitrobenzene 1.9‐solvate, C52H38N4O8·1.9C6H5NO2, (I). The solvent molecules are contained in extended channels which propagate through the host lattice between parallel screw/glide‐related columns of offset‐stacked porphyrin entities. Side packing of these columns involves π–π interactions between the methoxycarbonylphenyl residues. Molecules of the porphyrin host lie on crystallographic inversion centres. The zinc(II)–pyridine derivative pyridine(tetramethyl 4,4′,4′′,4′′′‐porphyrin‐5,10,15,20‐tetrabenzoato)zinc(II), [Zn(C52H36N4O8)(C5H5N)], (II), is a square‐pyramidal five‐coordinate complex with pyridine as an apical ligand, which crystallizes as a chloroform–pyridine solvate. The metalloporphyrin–pyridine units form an open layered arrangement, occluding the non‐coordinated solvent moieties within the intralayer interporphyrin voids. Within such arrays, the host porphyrin molecules are in contact with one another through the peripheral methoxycarbonyl substituents. The crystal packing consists of a bilayered arrangement of inversion‐related porphyrin layers, with the axial ligands mutually penetrating into the voids of neighbouring arrays and tight offset stacking of these bilayers. 相似文献
13.
Frank J. Feher Richard K. Baldwin Joseph W. Ziller 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(6):633-634
The crystal structure of the title complex, (η6‐hexamethylbenzene)bis(trifluoromethanesulfonato‐O)(2,4,6‐trimethylaniline‐N)ruthenium(II), [Ru(CF3O3S)2(C12H18)(C9H13N)], is described. The complex has the classic three‐legged piano‐stool structure with a planar arene 1.667 Å from the metal, two monodentate O‐bound trifluoromethanesulfonate ligands [Ru—O 2.169 (2) and 2.174 (2) Å] and one N‐bound mesidine ligand [Ru—N 2.198 (2) Å]. The Ru—N distance is relatively long and the average Ru—O distance is relatively short when compared with previously characterized RuII complexes. 相似文献
14.
Xia Li Ying‐Quan Zou Hai‐Bin Song 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(3):m110-m111
Each La3+ ion in the title complex, tetra‐μ‐2‐fluorobenzoato‐κ10O:O′;O:O,O′;O:O′;O,O′:O′‐bis[aqua(4,4′‐bipyridine‐κN)(2‐fluorobenzoato‐κO)lanthanum(II)], [La(C7H4FO2)6(C10H8N2)2(H2O)2], is coordinated by six O atoms from the carboxylate groups of five 2‐fluorobenzoate ligands, one O atom from a water molecule and one N atom from a 4,4′‐bipyridine molecule, thus forming a dimeric molecule. An infinite one‐dimensional dimeric supramolecular chain is formed via intermolecular hydrogen bonds. 相似文献
15.
Veysel T. Yilmaz Sema Caglar William T. A. Harrison 《Acta Crystallographica. Section C, Structural Chemistry》2004,60(1):m35-m38
The structures of trans‐bis[2‐(aminomethyl)pyridine‐κ2N,N′]bis(saccharinato‐κN)zinc(II), [Zn(C7H4NO3S)2(C6H8N2)2], (I), and [2‐(aminoethyl)pyridine‐κ2N,N′]bis(saccharinato‐κN)zinc(II), [Zn(C7H4NO3S)2(C7H10N2)], (II), exhibit octa‐ and tetrahedrally coordinated ZnII atoms, respectively. The diamine ligands behave as N,N′‐bidentate ligands, while saccharinate (sac) is coordinated through the N atom. In (I), the complex lies about an inversion centre with the Zn atom disordered and displaced by 0.256 (2) Å from a centre of symmetry towards a sac N atom. The crystal structure of (I) is stabilized by N—H⋯O hydrogen bonds and the crystal packing of (II) is determined by hydrogen bonding as well as weak π–π stacking interactions between the sac ligands. 相似文献
16.
Yoshio Wada Nobuo Okabe Yasunori Muranishi 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(10):m511-m513
In trans‐bis(5‐n‐butylpyridine‐2‐carboxylato‐κ2N,O)bis(methanol‐κO)copper(II), [Cu(C10H12NO2)2(CH4O)2], the Cu atom lies on a centre of symmetry and has a distorted octahedral coordination. The Cu—O(methanol) bond length in the axial direction is 2.596 (3) Å, which is much longer than the Cu—O(carboxylate) and Cu—N distances in the equatorial plane [1.952 (2) and 1.977 (2) Å, respectively]. In mer‐tris(5‐n‐butylpyridine‐2‐carboxylato‐κ2N,O)iron(III), [Fe(C10H12NO2)3], the Fe atom also has a distorted octahedral geometry, with Fe—O and Fe—N bond‐length ranges of 1.949 (4)–1.970 (4) and 2.116 (5)–2.161 (5) Å, respectively. Both crystals are stabilized by stacking interactions of the 5‐n‐butylpyridine‐2‐carboxylate ligand, although hydrogen bonds also contribute to the stabilization of the copper(II) complex. 相似文献
17.
Orde Q. Munro Greville L. Camp 《Acta Crystallographica. Section C, Structural Chemistry》2003,59(4):m132-m135
(Diphenyl phosphite‐κO)(5,10,15,20‐tetraphenylporphyrinato‐κ4N)manganese(III) hexafluoroantimonate(V), [Mn(C44H28N4)(C12H11O3P)](SbF6), is the first example of a structurally characterized diaryl or dialkyl phosphite complex of a metal–porphyrin ion. The axial phosphite ligand binds to the MnIII ion via the P=O O atom, affording a nominally five‐coordinate complex with an Mn—O distance of 2.120 (4) Å. The mean porphyrin Mn—N distance is 2.000 (4) Å and the MnIII ion is displaced from the 24‐atom porphyrin mean plane by 0.1548 (13) Å towards the axial O atom. The porphyrin adopts a marked saddle conformation, with a small domed component. The saddle distortion of the porphyrin ligand reflects the tight back‐to‐back dimers formed in the lattice by pairs of neighboring cations. The `non‐covalent' dimers in the lattice exhibit an unusual (weak) η2‐type coordination of a pyrrole C=C bond from a neighboring molecule, with MnIII⃛C distances of 3.697 (5) and 3.537 (5) Å. 相似文献
18.
Chengbing Ma Cheng Fan Changneng Chen Qiutian Liu 《Acta Crystallographica. Section C, Structural Chemistry》2002,58(11):m553-m555
In the title compound [systematic name: aqua(1,10‐phenanthroline‐κ2N,N′)(pyridine‐2,6‐dicarboxylato‐κ3O2,N,O6)manganese(II) monohydrate, [Mn(C7H3NO4)(C12H8N2)(H2O)]·H2O, the manganese(II) centre is surrounded by one bidentate phenanthroline ligand [Mn—N = 2.248 (3) and 2.278 (3) Å], one tridentate dipicolinate ligand [Mn—N = 2.179 (3) Å, and Mn—O = 2.237 (2) and 2.266 (2) Å] and one water molecule [Mn—O = 2.117 (3) Å], and it exhibits a strongly distorted octahedral geometry, with trans angles ranging from 144.12 (9) to 158.88 (11)°. Extensive intermolecular hydrogen‐bonding interactions involving coordinated and uncoordinated water molecules and the carboxyl O atoms of the dipicolinate ligand, as well as a stacking interaction involving the phenanthroline rings, are observed in the crystal structure. 相似文献
19.
Seong Huh Young Jun Park Alan. J. Lough Moo‐Jin Jun 《Acta Crystallographica. Section C, Structural Chemistry》2000,56(4):416-417
The title compound, [RuH(C6H8BN4)(C21H21P)2(CO)], possesses two trans‐disposed tri‐p‐tolylphosphines in axial positions and the remaining ligands in equatorial positions. The overall geometry of the RuII ion is a distorted octahedral structure. The P—Ru—P axis deviates from linearity by about 13°. This distortion arises mainly from the steric congestion between the bulky phosphine moieties and the tetrahedral dihydrobis(pyrazol‐1‐yl)borate ligands. 相似文献
20.
M. Enriqueta Díaz de Vivar Sergio Baggio María Teresa Garland Ricardo Baggio 《Acta Crystallographica. Section C, Structural Chemistry》2007,63(3):m123-m125
catena‐Poly[[[tetraaquazinc(II)]‐μ‐4,4′‐bipyridine‐κ2N:N′] [[μ‐thiosulfato‐κ2O:S‐bis[(thiosulfato‐κS)zinc(II)]]‐di‐μ‐4,4′‐pyridine‐κ4N:N′] dihydrate], {[Zn(C10H8N2)(H2O)4][Zn2(S2O3)3(C10H8N2)2]·2H2O}n, is a polymeric zinc complex built up from thiosulfate‐containing anionic chains, where the Zn atom is tetrahedrally coordinated, and aqua‐containing cationic chains incorporating octahedrally coordinated Zn. In each type of chain, the 4,4′‐bipyridine units act as spacers, and the chains run along three non‐intersecting almost orthogonal directions in space. The profusion of hydrogen‐bond donors (all the H atoms of the water molecules) and acceptors (the thiosulfate O and S atoms) generates a very complex hydrogen‐bonding scheme. 相似文献