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1.
The crystal and molecular structure of the complex containing cobalt-carbon and iron-sulfur cluster cores, (μ-p-CH3C6H4C2S) (μ-n-C3H7S)Fe2(CO)6Co2(CO)6, has been determined by X-ray diffraction method. The crystals are triclinic, space group P&1bar;, with a — 9.139(2), b=9.610(1), c-17.183(2) Å, α = 84.36(1), β-89.45(1), γ=88.15(1)°, V-1501.0 Å3; Z=2, Dc=1.74 g/cm3. R=0.072, Rw=0.081. The results of the structure determination show a cobalt-carbon cluster core formed through the reaction of (μ-p-CH3C6H4C2S)(μ-n-C3H7S)Fe2(CO)6 with Co2(CO)8. In the cobalt-carbon cluster core, the bond length of the original C≡C lengthened to 1.324 Å which is close to the typical value of carbon-carbon double bond. The groups connecting the carbons of the cluster core are in cis position and lie on the opposite side of cobalt atoms. In this complex, the conformation of —SC3H7 is e-type, while that of —SC2C6H4CH3 is a-type. 相似文献
2.
ResearchonCrystalStructureoftheComplexof10-Hydroxy-10-(3-indolyl)-9-phenanthrenonewithTetrahydrofuranMengJi-Ben;WenZhong;Wang... 相似文献
3.
Guang-Ming Yang Peng Cheng Dai-Zheng Liao Zong-Hui Jiang Shi-Ping Yan Geng-Lin Wang Xin-Kan Yao Hong-Gen Wang 《Journal of Cluster Science》1998,9(4):465-471
The preparation, magnetic properties, and crystal structure of [(salen)Cu]4[(salen)Fe(H2O)2]2(ClO4)2 via hydrogen bonding are described [salen=N,N-ethylenebis (salicylideneiminate)]. Crystals are triclinic, of space group
, with cell constants a=12.853(3), b=13.921(3), c=14.251(3) Å, =68.68(3)°, =87.86(3)°, =86.82(3)°, and Z=1. The structure was solved and refined to R=0.064 and R=0.068. The structure comprises the hexanuclear units which result from the linking of four mononuclear fragments [(salen)Cu] and two mononuclear fragment [(salen)Fe(H2O)]+, through Cu -O H -O -Fe -O -H O -Cu hydrogen bonds of coordinating H2O. In this complex, FeIII ions are in almost square-planar surroundings. The temperature dependences of the magnetic susceptibilities of the complex have been studied in the 4.2–300 K range, indicating the presence of an antiferromagnetic interactions between metal ions. 相似文献
4.
Ji-Ben Meng Mei-Qen Shen Xiao-Hong Wang Chen-Heng Kao Ru-Ji Wang Hong-Gen Wang Teruo Matsuura 《Journal of heterocyclic chemistry》1991,28(6):1481-1484
A number of fluorescent 3-aryl-1-methylquinolinones 3 were synthesized by the regiospecific photocoupling reaction of 3-halo-1-methylquinolinones 1 with aromatic and heteroaromatic compounds 2 . An unusual photocoupling product 4 was obtained in the photolysis of 3-iodo-1-methylquinolinone in the presence of benzene. The structure of 4 was unequivocally established by an X-ray crystallographic analysis. 相似文献
5.
The mononuclear vanadium(Ⅴ) complex with 2-hydroxyl-1-naphthaldehyde isoncotinoyl hydrazone was synthesized and characterized by single-crystal X-ray diffraction.The crystal is of monoclinic,space group P2 1/n with a = 10.3153(15),b = 7.4024(11 ),c = 24.413(4) (A),β= 101.911(2)°,V= 1824.0(5) (A)3,Z = 4,Mr = 427.28,Dc = 1.556 g/cm3,F(000) = 880,μ(MoKα) =0.591,the final R = 0.0372 and wR = 0.0926.The vanadium(Ⅴ) atom adopts a distorted square-pyramidal geometry coordinated by the tridentate ligand and two oxygen atoms.The hydrogen bonds and strong π…π stacking interactions link the complex molecules into a 3-D network structure. 相似文献
6.
Photocycloadditionof(4-methyl-7-coumarinyl)OxyaceticAcidPropanediolDiesterandX-rayCrystalStructureofProductDuDa-Ming;WangYong... 相似文献
7.
Feng Ke-Sheng Chen Ru-YuInstitute of Elemento-Organii Chemistry Nankai University Tianjin Wang Hong-Gen Wang Ru-JiCentral laboratory Nankai University Tianjin 《结构化学》1993,(5)
<正> Crystal of the title compound Mr=304. 80 belongs to the triclinic, space group P1, with a = 7. 282)2), b=9. 064(2), c=11. 737(5) A , α=75. 79 (3), β=78. 70(3), γ=88. 49(2)°, V-736. 21 A3, Z=2, Dx = l. 375 g/cm3. The final refinement is converged with R=0. 062 and Rw= 0. 069.The five-membered heterocycle is in envelope conformation. The P - N bond length (1. 68(1)) indicates that the dπ-Pπ bond between P and N of the title compound is stronger than that of the corresponding 4-phenyl compound. 相似文献
8.
1 INTRODUCTIONOrganophosphorus compounds are ubiquitous in nature and they have broad applications in the fields of agriculture and medicine. During the past two decades, (-ketophosphonates and their derivatives have attracted considerable attention because these compounds are endowed with special physical, chemical and pharmacological properties due to the proximity of the carbonyl and the phosphoryl groups[1~6]. For example, it is well known that phosphonoformic acid (PFA) is effectiv… 相似文献
9.
The title compound has been synthesized and its crystal structure was determined by X-ray crystallographic method. The crystal is triclinic, space group P-1, with unit cell dimensions a = 6.146 (5), b = 8.473(6), c = 14.383(5) Å; α = 77.47 (4), β = 82.84 (4), γ = 69.00 (8)° and Z = 2. The results obtained reveal that the molecule of the title compound keeps a long conjugative system involving CC double bond, cyclopropane ring, carbonyl group and isoxazolinone ring and adopts a low energy conformation including s-trans of CC double bond, s-cis of carbonyl group with respect to the three-membered ring and like-s-trans of carbonyl group with the carbonyl group within the heterocyclic moiety. 相似文献
10.
合成了12种稀土金属硫氰酸盐与N-对氯苯基氮杂15-冠-5的固体配合物,进行了元素分析和电导、红外光谱、电子光谱测定及热重-差热分析,并对Sm(SCN)3·L作了X射线单晶结构分析,结果表明:Sm(Ⅲ)离子与冠醚上的5个杂原子及3个硫氰酸根上的氮原子配位,配位数为8. 相似文献