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1.
Stash A. I. Perepelkova T. I. Noskov Yu. G. Buslaeva T. M. Romm I. P. 《Russian Journal of Coordination Chemistry》2001,27(8):585-590
Palladium clusters Pd4(SEt)4(OAc)4(I) and Pd6(SEt)12(II) were synthesized and studied. Their structure was determined by X-ray diffraction analysis. For I, a= 9.774(2) Å, b= 10.821(2) Å, c= 13.061(3) Å, = 92.88(3)°, V= 1379.6(5) Å3, (calcd.) = 2.182 g/cm3, space group P21/n, Z= 4, N
ref= 1558, and R= 0.031; for II, a= 10.581(1) Å, b= 10.584(2) Å, c= 11.478(2) Å, = 101.62(1)°, = 104.95(1)°, = 106.74(1)°, V= 1135.2(4) Å3, (calcd) = 2.007 g/cm3, space group P1, Z= 1, N
ref= 2828, and R= 0.022. In cluster I, four Pd atoms form a planar cycle. The neighboring palladium atoms are bound by two acetate or by two mercaptide bridges, the Pd···Pd distances being 3.036–3.195 Å. In cluster II, Pd atoms form a planar six-membered cycle with Pd···Pd distances of 3.083–3.127 Å. The neighboring palladium atoms are bound by two mercaptide bridges. The formation of analogous clusters in solution was confirmed by IR spectroscopy. 相似文献
2.
Kosterina E. V. Troyanov S. I. Aslanov L. A. Kemnitz E. 《Russian Journal of Coordination Chemistry》2001,27(8):527-536
By reacting the K, Rb, Cs, or Tl carbonates with excess phosphoric acid, crystals of superacid phosphites, namely, (RbH2PO3)2· H3PO3(I), (TlH2PO3)2· H3PO3(II), KH2PO3· H3PO3(III), -CsH2PO3· H3PO3(IV), and -CsH2PO3· H3PO3(V), were synthesized. Their structures were determined by single-crystal X-ray diffraction analysis at 150 K. Crystals I: triclinic system, space group
, a= 7.713(2) Å, b= 8.679(3) Å, c= 9.235(3) Å, = 79.36(3)°, = 67.60(2)°, = 88.13(3)°, R
1= 0.0252; crystals II: triclinic system, space group
, a= 7.690(3) Å, b= 8.494(3) Å, c= 9.292(4) Å, = 79.48(3)°, = 66.72(3)°, = 85.45(3)°, R
1= 0.0485; crystals III: monoclinic system, space group P21/c, a= 8.726(3) Å, b= 12.182(4) Å, c= 6.354(2) Å, = 104.14(3)°, R
1= 0.0241; crystals IV: orthorhombic system, space group P212121, a= 6.033(1) Å, b= 6.444(1) Å, c= 18.345(4) Å, R
1= 0.0172; crystals Vare monoclinic, space group C2/c, a= 9.990(3) Å, b= 12.197(4) Å, c= 6.866(2) Å. = 118.14(3)°, R
1= 0.0181. The hydrogen bonding systems form corrugated bands (Iand II), bent layers (III), individual tubes with rectangular cross sections (V), or a three-dimensional framework (IV). A comparative analysis of the crystal structures of acid phosphites with different compositions was performed. 相似文献
3.
On the crystal chemistry of three copper(II)-arsenates: Cu3(AsO4)2-III,Na4Cu(AsO4)2, and KCu4(AsO4)3
Herta Effenberger 《Monatshefte für Chemie / Chemical Monthly》1988,119(10):1103-1112
The three copper(II)-arsenates were synthesized under hydrothermal conditions; their crystal structures were determined by single-crystal X-ray diffraction methods:Cu3(AsO4)2-III:a=5.046(2) Å,b=5.417(2) Å,c=6.354(2) Å, =70.61(2)°, =86.52(2)°, =68.43(2)°,Z=1, space group
,R=0.035 for 1674 reflections with sin / 0.90 Å–1.Na4Cu(AsO4)2:a=4.882(2) Å,b=5.870(2) Å,c=6.958(3) Å, =98.51(2)°, =90.76(2)°, =105.97(2)°,Z=1, space group
,R=0.028 for 2157 reflections with sin / 0.90 Å–1.KCu4(AsO4)3:a=12.234(5) Å,b=12.438(5) Å,c=7.307(3) Å, =118.17(2)°,Z=4, space group C2/c,R=0.029 for 1896 reflections with sin / 0.80 Å–1.Within these three compounds the Cu atoms are square planar [4], tetragonal pyramidal [4+1], and tetragonal bipyramidal [4+2] coordinated by O atoms; an exception is the Cu(2)[4+1] atom in Cu3(AsO4)2-III: the coordination polyhedron is a representative for the transition from a tetragonal pyramid towards a trigonal bipyramid. In KCu4(AsO4)3 the Cu(1)[4]O4 square and the As(1)O4 tetrahedron share a common O—O edge of 2.428(5) Å, resulting in distortions of both the CuO4 square and the AsO4 tetrahedron. The two Na atoms in Na4Cu(AsO4)2 are [6] coordinated, the K atom in KCu4(AsO4)3 is [8] coordinated by O atoms.Die drei Kupfer(II)-Arsenate wurden unter Hydrothermalbedingungen gezüchtet und ihre Kristallstrukturen mittels Einkristall-Röntgenbeugungsmethoden ermittelt:Cu3(AsO4)2-III:a = 5.046(2) Å,b = 5.417(2) Å,c = 6.354(2) Å, = 70.61 (2)°, = 86.52(2)°, = 68.43(2)°,Z = 1, Raumgruppe
,R = 0.035 für 1674 Reflexe mit sin / 0.90 Å–1.Na4Cu(AsO4)2:a = 4.882(2) Å,b = 5.870(2) Å,c = 6.958(3) Å, = 98.51(2)°, = 90.76(2)°, = 105.97(2)°,Z = 1, Raumgruppe
,R = 0.028 für 2157 Reflexe mit sin / 0.90 Å–1.KCu4(AsO4)3:a = 12.234(5) Å,b = 12.438(5) Å,c = 7.307(3) Å, = 118.17(2)°,Z = 4, Raumgruppe C2/c,R = 0.029 für 1896 Reflexe mit sin / 0.80 Å–1.Die Cu-Atome in diesen drei Verbindungen sind durch O-Atome quadratisch planar [4], tetragonal pyramidal [4 + 1] und tetragonal dipyramidal [4 + 2]-koordiniert; eine Ausnahme ist das Cu(2)[4 + 1]-Atom in Cu3(AsO4)2-III: Das Koordinationspolyeder stellt einen Vertreter des Übergangs von einer tetragonalen Pyramide zu einer trigonalen Dipyramide dar. In KCu4(AsO4)3 haben das Cu(1)[4]O4-Quadrat und das As(1)O4-Tetraeder eine gemeinsame O—O-Kante von 2.428(5) Å, was eine Verzerrung der beiden Koordinationsfiguren CuO4-Quadrat und AsO4-Tetraeder bedingt. Die zwei Na-Atome in Na4Cu(AsO4)3 sind durch O-Atome [6]-koordiniert, das K-Atom in KCu4(AsO4)3 ist [8]-koordiniert.
Zur Kristallchemie dreier Kupfer (II)-Arsenate: Cu3(AsO4)2-III, Na4Cu(AsO4)2 und KCu4(AsO4)3相似文献
4.
Two novel heterometallic cubane-like and double cubane-like clusters, {MoCu3S3(S2COEt)}(O)(Ph3P)3
I and {Mo2Cu6S6(SCMe3)2}(O)2(Ph3P)4
II, were synthesized by reaction of {MoCu2S3}(O)(Ph3P)3 with CuS2COEt and CuSCMe3, respectively. ClusterI crystallized in the triclinic space group
(2) witha=12.766(6) Å,b=22.904(5) Å,c=10.522(3) Å, =99.86(2)°, =109.68(2)°, =86.84(3)°,V=2854(2) Å3,Z=2,R=0.049 for 6622 observed reflections (I>5(I)) and 410 variables. ClusterII crystallized in the triclinic space group
(2) with dimensionsa=14.212(4) Å,b=14.725(5) Å,c=12.396(8) Å, =110.32(4)°, =90.40(5)°, =62.88(2)°,V=2129(2) Å3,Z=1,R=0.039 for 6020 observed reflections (I>3(I)) and 461 variables. ClusterI consists of a neutral cubane-like molecule with the core {MoCu3S3(S2COEt)}2+, in which one corner of the cubane-like core is a novel triply bridging bidentate 1,1-dithiolato (xanthate, S2COEt–) ligand. ClusterII is a double cubane-like one, in which two cubane-like cores {MoCu3S3(SCMe3)}2+ are connected by two Cu-S bonds of the triply bridging monothiolato (SCMe
3
–
) ligand. Two different pathways of unit construction from a small heterometallic cluster {MoCu2S3}(O)(Ph3P)3 have been outlined. Comparisons of the selected bond lengths and bond angles for the cubane-like core {MoCu3S3
X} (X=Cl–, Br–, S2COEt–, SCMe
3
–
) are given. Spectroscopic properties of the title clusters are also reported. 相似文献
5.
Herta Effenberger 《Monatshefte für Chemie / Chemical Monthly》1986,117(10):1099-1106
Crystals of PbCu3(OH)(NO3)(SeO3)3·1/2H2O [a=7.761(3)Å,b=9.478(4)Å,c=9.514(4)Å, =66.94(2)°, =69.83(2)°, =81.83(2)°, space group P
,Z=2] and Pb2Cu3O2(NO3)2(SeO3)2 [a=5.884(2)Å,b=12.186(3)Å,c=19.371(4)Å, space group Cmc21,Z=4] were synthesized under hydrothermal conditions. Their crystal structures were refined with three-dimensional X-ray data toR
w=0.033 resp. 0.055. In PbCu3(OH)(NO3)(SeO3)3·1/2H2O the Cu atoms are [4+1] and [4+2] coordinated and via SeO3 groups a three-dimensional atomic arrangement is built up. In Pb2Cu3O2(NO3)2(SeO3)2 there are
sheets, which are connected only via Pb-O bonds ranging from 2.98 Å to 3.16 Å. 相似文献
6.
Budantseva N. A. Andreev G. B. Fedoseev A. M. Antipin M. Yu. 《Russian Journal of Coordination Chemistry》2004,30(10):713-717
A new complex of Np(V) [NpO2(HCOO){OC(NH2)2}3] (I) was synthesized and its crystal structure was determined: a = 6.674(1) Å, b = 13.164(2) Å, c = 7.020(1) Å, = 101.35(1)°, space group P21, Z = 2, V = 604.7(2) Å3, R = 0.048, wR(F
2) = 0.128. The structure consists of infinite chains of [NpO2(HCOO){OC(NH2)2}3]. The coordination polyhedron of the Np atom is a pentagonal bipyramid with the O atoms of three carbamide molecules and two formate ions in the equatorial plane. The absorption spectra were measured in IR and near-IR regions for compound I and for the [NpO2Cl{OC(NH2)2}4] complex, whose structure was reported in the previous publication. 相似文献
7.
The carbonylation of Os2(CO)10[-CH2N(Me)C(Et)](-H),1 at 110°C/1300 psi has yielded the carbene complex Os3(CO)11[C(Et)NMe2],2, the first simple carbene derivative of Os3(CO)12, in 68% yield. Compound2 was characterized by a single crystal structure analysis which showed the position of a dimethylaminocarbene ligand in an equatorial coordination site. Compound2 is decarbonylated at 97°C to reform1 in 59% yield. Compound1 can be decarbonylated further at 125°C to yield the new compound Os3(CO)9 [3-2-C(H)N(Me)C(Et)](-H)2,3 in 94% yield. Compound3 was characterized by a crystal structure analysis and was shown to possess a triply bridging C(H)N(Me)C(Et) ligand containing two carbene centers. Compounds1 and2 can be regenerated from3 by carbonylation with CO at 110°C/800 psi. The facile activation of the N-methyl CH bonds of the carbene ligand of2 is produced by the metal atoms adjacent to the carbene coordination site, and may be a characteristic feature of the chemistry of carbene ligands in clusters. For2: space group=P
,a=11.407(2) Å,b=12.332(2) Å,c=8.602(1) Å, =103.92(1), =110.56(1)°, =82.57(1),Z=2, 2627 reflections,R=0.031; for3: space group=C2/c,a=17.160(3) Å,b=8.947(2) Å,c=27.034(6) Å, =97.82(1)°,Z=8, 2044 reflections,R=0.038. 相似文献
8.
Udovenko A. A. Zemnukhova L. A. Gorbunova Yu. E. Mikhailov Yu. N. Davidovich R. L. 《Russian Journal of Coordination Chemistry》2002,28(1):12-14
The crystal structure of a novel antimony(III) fluoride complex, ammonium undecafluorotriantimonate(III) (NH4)2Sb3F11, was determined. The crystals are triclinic: a = 7.780(2) Å, b = 8.370(2) Å, c = 10.620(1) Å, = 71.06(1)°, = 89.03(1)°, = 63.58(1)°, V = 579.1(2) Å3, Z = 2, (calcd) = 3.500 g/cm3, (exp) = 3.51 g/cm3, F(000) = 548.0, space group P
. The structure consists of anionic [Sb3F11]2– chains and ammonium cations combined into a framework by the N–H···F hydrogen bonds. 相似文献
9.
X-ray crystal structure analyses of (CH3NCO)3 (M) and (ClNCO)3·1/2C2H4Cl2 (C) were carried out at room temperature (MoK, graphite monochromator, =0.71069 Å): 1.M=171.16, monochlinic, P21/c,a=14.848 (1) Å,b=13.400 (2) Å,c=8.149 (1) Å, =100.87 (1)°,V=1 592.3 Å3,Z=8,F(000)=720,d
x
=1.428 Mgm–3, =76m–1,R=6.51%,R
w
=7.01% (964 reflections, 218 parameters). 2.M=281.89, monochlinic, P 21/c,a=9.416 (3) Å,b=5.728 (1) Å,c=18.199 (8) Å, =98.64 (2)°,V=970.4 Å3,Z=4,F(000)=556,d
x
=1.929 Mgm–3, =1.11 mm–1,R=3.96%,R
w
=3.44% (605 reflections, 132 parameters). The ring systems together with the C atoms of the methyl groups in (M) and with the Cl atoms in (C) are planar and have D3h-symmetry. Bond lengths and bond angles are discussed with regard to14N-NQR,35Cl-NQR and vibrational spectroscopic data. 相似文献
10.
From the reaction or Mo2Cl6(THF)3 with excess of NaO2CPh and PEt3 in THF three types of crystals have been obtained and recrystallized in CH2Cl2. They are brown compound Mo2(O2CPh)6(PEt3)2·2CH2Cl2 (1), yellow-Mo2(O2CPb)4 (2), and black Mo4O6(O2CPh)6(PEt3)2.CH2Cl2 (3). When a strict ratio of MO2Cl6(THF)3:NaO2CPh = 1:2 was applied, Mo2(O2CPh)4(THF)2, (4) was the only compound separated from the THF reaction mixture. Their structures have been determined by X-ray crystallography. There are three coordination modes of benzoate in 1: bridging
2-O2CPh, bridging
1-O2CPh and terminal O2CPh groups. Compound 2 is chemically well known, but was found to pack differently from the previously reported structure. Mo4O6(O2CPh)6(PEt3)2·CH2C12 (3) is a mixed-valence Mo (IV, V) tetranuclear compound in a butterfly arrangement. A molecule of 4 is actually a MO2(O2CPh)4 molecule with two THIF molecules axially coordinating to the molybdenum atoms. The crystallographic data for these compounds are as follows: 1, triclinicPl witha = 11.612(3) Å, b = 11.970(2) Å,c=12.135(3) Å,=95.55(2)°,=117.51(2)°,98.84(2)°,V=l450.8(7) Å3,Z=1,R=0.0673, and R
w
,=0.0936; 2, monoclinicP21/n witha = 14,437(2) Å,b=5.6168(7) Å,c=15.979(3) Å,=93,93(l)°,V=1292.7(4) Å3,Z=2,R=0.0217, and Rw=0.0352; 3, trigonal (hexagonal setting)R3¯ witha=28.83(4) Å,c=44.98(2) Å,V=323570(10) Å3,Z=18,R=0.067, andwR2=0203; 4 monoclinicP21/c witha=9.456(4) Å,b=17.757(8) Å,c=10.887(3) Å,=109.63(2)°,V=1722(2)Å3
Z=2,R=0.0330, andR
w = 0.0451. 相似文献
11.
Weng Kee Leong Frederick W. B. Einstein Roland K. Pomeroy 《Journal of Cluster Science》1996,7(2):121-143
The complexes [(OC)4Os(PbMe2)]2 (3) and [(OC)4OsSnBu
2
]2 (4) have been prepared from be reaction of Na2[Os(CO)4] with Me2PbCl2 and Bu
2
SnCl2, respectively, in THF and their X-ray crystal structures determined. The red derivative,3, was light-sensitive in solution. The reactions or [(OC)4 Os(SnMe2)]2 (2), or its decarbonylated derivative [Os3(CO)7(SnMe2)2]2 (7), with olefins or phosphorus donor ligands have also been investigated, and the structures of two derivatives, viz. [Os2(CO)7(SnMe2)2(C2H4)] (5a) and [Os2(CO)7(SnMe2)2(PMe3)] (6a), have been determined; the noncarbonyl ligand occupies an equatorial site in each case. The X-ray crystal structures of all these compounds, like those of [(OC)4Os(EMe2)]2 (E=Ge (1), Sn (2)) which have been reported previously, show leaning of the axial carbonyl ligands toward the metal tetracycle, i.e., an umbrella effect. Crystallographic data for compound3: space group, P21/a;a=13.4404(13) Å,b=10.7494(14) A,c=148967(18) A,=98.204(9)°,R=0.035, 1983 observed reflections. For compound4: space group,P1;a=9.016(1) Å,b=9.370(1),c=11.334(1) A, =103.67(1)°,=100.30(1)°, =115.03(1)°, R=0.046, 2026 observed reflections. For compound5a: space group,P1;a=9.2933(11)Å,b=9.7181(3),c=12.2508(15) A, =89.21(1)°,=87.61(1)°, =86.13(1)°,R=0.038, 2770 observed reflections. For compound6a space groupP1:a=8.7244(9)Å,b=10.9318(6),c=13.2560(13) A, =87.815(6)°,=83.655(8)°, =82.343(6)°, R=0.030, 3497 observed reflections. 相似文献
12.
Henri Arzoumanian Marcel Pierrot Fouad Ridouane Jose Sanchez 《Transition Metal Chemistry》1991,16(4):422-426
Summary Several penta-and tetracyanooxomolybdenum(IV) anions have been synthesized containing different numbers of H2O molecules, either coordinated or present as crystallisation molecules. The influence of these molecules on the reactivity of the complex, especially towards O2, is discussed. Three compounds were characterized by x-ray structure determination. [Mo(O)(CN)5(H2O)2(MeCN)2][PPh4]4Cl belongs to triclinic space group P-1 witha=13.146(3) Å,b=16.944(5) Å,c=21.761(6) Å, =84.72(2)°, =87.15(2)° and =85.25(2)°. The volume of the unit cell is 4678(6)Å3 withz=2. The structure was refined to R=6.5%. [Mo(O)(CN)4(H2O)·6H2O][PPh4]2 belongs to monoclinic space group P21/n witha=15.313(2)Å,b=19.983(3)Å,c=17.006(2)Å, =100.51(2)°. The volume of the unit cell is 5117(3)Å3 withz=4. The structure was refined to R=8.7%. [Mo(O)(CN)4(MeCN)](PH3)2N]2 belongs to triclinic space group P-1 witha=13.770(4)Å,b=16.292(5)Å,c=16.889(5)Å, =73.23(2)°, =72.02(2)° and =71.57(2)°. The volume of the unit cell is 3342(3)Å3 withz=2. The structure was refined to R=7.2%. 相似文献
13.
The reaction of Ru3(CO)12 with 3,3 dimethylthietane (DMT) at 68°C yielded the new tetraruthenium cluster complex Ru4(CO)12(-SCH2CMe2CH2)2,1 in 23% yield. Compound1 was characterized crystallographically and was shown to consist of a puckered square of four ruthenium atoms with two DMT ligands bridging opposite sides of the cluster via the sulfur atoms. Compound1 reacts with CO (98°C/1 atm) to yield the new tetraruthenium complex Ru4(CO)13 (-SCH2CMe2CH2),2 in 69% yield. Compound2 consists of a butterfly tetrahedral cluster of four ruthenium atoms with a DMT ligand bridging the wing-tip metal atoms. Addition of DMT to2 regenerates1 in 67% yield. Crystal data—1: space group =
,a=17.490(2) Å,b=18.899(3) Å,c=9.781(1) Å, =93.06(1)°, =91.06(1)°, =105.239(9)°,Z=4, 5799 reflections,R=0.026; for2: space group = P21/n,a=15.430(3) Å,b=18.285(4) Å,c=9.850(2) Å, =90.05(2)°,Z=4, 2111 reflections,R=0.036. 相似文献
14.
E. M. Limanski M. Piepenbrink E. Droste K. Burgemeister B. Krebs 《Journal of Cluster Science》2002,13(3):369-379
Two novel examples of sandwich type heteropolyanions were synthesized and characterized by X-ray crystal structure and elemental analysis as well as infrared spectroscopy. Na13[H3Cu4(H2O)2(CuW9O34)2]39H2O (1) and Na9K[Fe4(H2O)2(FeW9O34)2]32H2O (2) were prepared in aqueous solution by reaction of sodium tungstate with FeIII and CuII cations, respectively. 1 crystallizes in the monoclinic space group P21/n (a=13.054(3) Å, b=17.729(4) Å, c=20.998(4) Å, =93.50(3)°), while 2 is triclinic, space group P¯1 (a=12.316(2) Å, b=13.716(3) Å, c=14.925(3) Å, =99.36(3)°, =104.21(3)°, =101.55(3)°). Each anion consists of two [XW9O34]
n– moieties (X=FeIII, n=11 (1) and CuII, n=12 (2)) which can be described as -B-isomers of the defect Keggin anion. These units are linked via a belt of four FeIIIO6 or CuIIO6 groups. Two transition metal atoms fill their octahedral coordination sphere with one additional water ligand. 相似文献
15.
Udovenko A. A. Zemnukhova L. A. Kovaleva E. V. Gorbunova Yu. E. Mikhailov Yu. N. 《Russian Journal of Coordination Chemistry》2004,30(8):550-554
The crystal structures of complex antimony(III) fluorides RbSbF4 (I) and (C2N4H5)SbF4 (II) were determined. The crystals of I and II are monoclinic; for I: a = 4.628(1) Å, b = 6.167(1) Å, c = 7.922(1) Å, = 100.582(3)°, V = 222.24(7) Å3, Z = 2, (calcd.) = 4.23 g/cm3, (exp.) = 4.25 g/cm3, F(000) = 248, space group P21/m, R = 0.0395; for II: a = 4.678(1) Å, b = 7.339(4) Å, c = 10.185(1) Å, = 90.88(2)°, V = 349.6(2) Å3, Z = 2, (calcd.) = 2.69 g/cm3, (exp.) = 2.70 g/cm3, F(000) = 264, space group P21. The structure of I is formed by Rb+ cations and [SbF4]
n–
n
anionic chains composed of SbF5E octahedra with two bridging fluorine atoms. The structure of IIis formed by (C2N4H5)+ cations and isolated [SbF4]– anions in which the antimony polyhedra are SbF4E trigonal bipyramids. The relationship between the crystal structures and electrophysical and biological properties of single-charged cation tetrafluoroantimonates(III) was studied. 相似文献
16.
G. Giester 《Monatshefte für Chemie / Chemical Monthly》1996,127(4):347-354
Summary The new synthetic compound ZnFe
2
3+
(SeO3)4 forms at low-hydrothermal conditions at 220 °C. It belongs to the monoclinic system; the structure was determined by single-crystal X-ray diffraction in the space group Pc. The unit cell data are:a=8.196(4) Å,b=7.997(4) Å,c=8.033(4) Å, =92.27(3)°,V=526.1 Å3;Z=2. The structure of ZnFe
2
3+
(SeO3)4 contains two types of FeO6 octahedra, one distorted ZnO5 trigonal bipyramid, and four selenite groups. Formal clusters consisting of the ZnO5 group, edge-linked with both FeO6 groups and one SeO3 pyramid, are connected by common corners, involving three further selenite groups to a framework structure.
Die Kristallstruktur von ZnFe 2 3+ (SeO3)4
Zusammenfassung Die neue synthetische Verbindung ZnFe 2 3+ (SeO3)4 bildet sich bei niedrighydrothermalen Bedingungen (220°C). Die Kristallstruktur wurde mit Einkristallröntgenmethoden in der monoklinen Raumgruppe Pc gelöst. Die Zellparameter sind:a=8.196(4) Å,b=7.997(4) Å,c=8.033(4) Å, =92.27(3)°,V=526.1 Å3;Z=2. Die Kristallstruktur von ZnFe 2 3+ (SeO3)4 weist zwei Arten von FeO6-Oktaedern, eine verzerrte trigonale ZnO5-Dipyramide sowie vier Selenitgruppen auf. Formal können Cluster, bestehend aus dem ZnO5-Polyeder, kantenverknüpft mit den beiden FeO6-Gruppen sowie einer SeO3-Pyramide, beschrieben werden. Die Verknüpfung über Ecken zu einer Gerüststruktur erfolgt unter Beteiligung von drei weiteren Selenitgruppen.相似文献
17.
G. B. Andreev M. Yu. Antipin N. A. Budantseva E. V. Tuchina L. B. Serezhkina A. M. Fedoseev A. B. Yusov 《Russian Journal of Coordination Chemistry》2004,30(12):868-873
A complex of uranyl perchlorate with imidazolidine-2-one as the molecular ligand, [UO2(Imon)4(H2O)](ClO4)2 (I), was synthesized and structurally characterized by X-ray diffraction analysis. The coordination number of the uranium atom is 7. The nearest environment of the uranyl ion includes four O atoms of the imidazolidine-2-one molecules and one O atom of the water molecule. The perchlorate anions are outer-sphere ligands. The crystals are monoclinic: space group P21/c; a = 16.294(3) Å, b = 16.135(3) Å, c = 9.987(2) Å, = 97.69 (3)°, V = 2603.0 (9) Å3, (calcd) = 2.117 g/cm3, Z = 4. The IR and luminescence spectra of the complex were recorded.Translated from Koordinatsionnaya Khimiya, Vol. 30, No. 12, 2004, pp. 919–924.Original Russian Text Copyright © 2004 by Andreev, Antipin, Budantseva, Tuchina, Serezhkina, Fedoseev, Yusov. 相似文献
18.
Thomas C. W. Mak Richard K. McMullan 《Journal of inclusion phenomena and macrocyclic chemistry》1988,6(5):473-481
The title ternary complexes (1, X=Cl;2, X=Br;3, X=CN) have been prepared and characterized by X-ray crystallography. Crystal data: space groupP21/n,Z=4;1,a=7.505(2),b=14.556(4),c=14.453(3) Å, =98.13(2)o, andR
F=0.088 for 1831 observed MoK
data;2,a=7.483(1),b=14.643(6),c=14.443 Å, =98.25(2)o, andR
F=0.113 for 923 data;3,a=7.490(2),b=14.646(5),c=14.594(5) Å, =98.85(5)o, andR
F=0.082 for 915 data. In the isomorphous crystal structure of1 and2, ordered (C2H5)4N+ cations are sandwiched between puckered layers matching the (020) family of planes, each being constructed from the cross-linking of planar zigzag chains of hydrogen-bonded urea molecules by the water molecules and halide ions. Compound3 has the same structure except that its cyanide group is disordered.
Supplementary Data relating to this article are deposited with the British Library as Supplementary Publication No. SUP 82066 (30 pages).Operated under contract DE-AC02-76CH00016 with the U.S. Department of Energy, Office of Basic Energy Science. 相似文献
19.
Pierre Braunstein Chantal Charles Richard D. Adams Ralph Layland 《Journal of Cluster Science》1996,7(2):145-154
The reaction of the siloxyl containing ferrate [Fe(CO)3(
1-dppm){Si(OMe)3}]–,1 (dppm = Ph2PCH2PPh2) with Sn(OAc)2(n-Bu)2 has yielded the new dimeric complex [Fe(CO)3(
1-dppm){µ-Sn(n-Bu)2}]2, 3 in 89% yield. Compound3 was characterized crystallographically and was found to be a centrosym-etrical molecule with a rhomboidal Fe2Sn2 cluster at the center. Each iron atom contains me
1-dppm ligand. Compound3 was found to react with [Pd(dmba) (µ-Cl)]2 (dmba=dimethylbenzylamine) to yield the new complexmer-[Fe(CO)3{Sn(n-Bu)2}(µ-dppm)Pd(dmba)Cl]2, 4 by attachment of a palla-dium grouping to each of the uncoordinated phosphorus atoms in 3. Crystal data for 3: space groupP
,a=11.399(2) Å, 6=15.98(3) Å, c=10.869(3) Å, =94.10(2)°.=100.56(2)°, =69.35(1)°,Z=2, 3533 reflections,R=0.034. 相似文献
20.
Summary Os2(CO)8Cl2
(1) is orthorhombic P212121 witha=9.3599(9),b=9.879(2),c=16.014(3), V=14803, Dc=3.03 Mgm–3 for Z=4. Structure solved by Patterson methods. Final R=0.038, Rw=0.038 [w=(2F)] for 1270 observed reflections and 141 parameters. Os3(CO)12Cl2
(2) is monoclinic C2/m witha=12.105(3), b=10.612(3),c=8.798(1) , =117.02(2)°, V=10063, Dc=3.22 Mgm–3 for Z=2. Structure solved by Patterson methods. Final R=0.036, Rw=0.037 (w=(2F)–) for 821 observed reflections and 75 parameters.Complex(1) has an osmium-osmium single bond 2.897(1), with the chloride ligands in equatorial positions,(2) has a linear triosmium chain with osmium-osmium single bonds 2.893(1) and the chloride ligands occupy equatorial sites on the terminal osmium atoms. Both(1) and(2) are isostructural with their osmium carbonyl iodide analogues. 相似文献