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1.
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
2.
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
3.
The crystal structure of an unusual dimeric Ni(II) complex with 3-imidazoline nitroxide LH=C9H14N2O2 of the formula Ni2(LH)4 has been determined. The structure is molecular, space group P21/c, with a=12.150(3) Å, b=11.229(3) Å, c=15.780(4) Å, =101.59(3)o, and d
calc
=1.54 g/cm3, for Z=2; V=2109(1) Å3, R=0.059. In the centrosymmetric dimer, the Ni...Ni distance is 3.254(2) Å; the coordination polyhedron of Ni is a square pyramid (the coordination number is 5) formed by the donor O and N atoms of LH ligands acting as the bidentate-cyclic and bidentate bridged-cyclic structures. The Ni–O and Ni–N distances are 1.989(7) and 2.032(8) Å, respectively (for the atoms forming the pyramid base), and 2.000(8) Å to the apical N atom. The Ni atom is displaced from the base to the apex of the pyramid by 0.35 Å. The interatomic distances and the bond angles in the ligands agree with those for the previously studied M(LR)2 complexes. The distances between the Ni(II) ions and the
O O atoms inside the Ni(LH)2 fragments are 5.39(1) and 5.45(1) Å, the intermolecular Ni...O distances exceed 6 Å, and the O...O distances are as long as 4.73(1) Å.Institute of Inorgamic Chemistry, Siberian Branch, Russian Academy of Sciences. Translated fromZhurnal Stukturnoi Khimii, Vol. 34, No. 3, pp. 80–85, May–June 1993.Translated by T. Yudanova 相似文献
4.
Ahmed A. Mohamed José M. López-de-Luzuriaga John P. Jr. Fackler 《Journal of Cluster Science》2003,14(1):61-70
The tetranuclear Au(I) pyrazolate complex, [(dppm)2Au4(3,5-Ph2Pz)2](NO3)2 H2O, 1, has been synthesized and structurally characterized. It is the first tetranuclear pyrazolate of Au(I) to have been found, although the trinuclear pyrazolates of Au(I) are well known. Complex 1 exhibits luminescence at 77 K when excited at 333 nm with an emission maximum at 454 nm. The emission has been assigned to ligand to metal charge transfer, LMCT, based upon the vibronic structure that is observed. The complex crystallizes in the monoclinic space group P21/c, with a=19.33(3) Å, b=20.26(3) Å, c=19.80(3) Å, =106.74(2)°, V=7425(17) Å3, Z=8, and R=0.058. The Au Au distances are Au(1) Au(4)=3.185(3) Å, Au(1) Au(2)=3.230(3) Å, Au(2) Au(3)=3.079(3) Å, and Au(3) Au(4)=3.280(3) Å. 相似文献
5.
The complexes [Et4N][(Ph3P)2{MS2
MS2Fe}Cl2] (M=Mo,M=Ag;M=W,M=Cu, Ag) have been obtained by reaction of [Et4N]2[S2
MS2FeCl2] (M=Mo, W) with Cu(PPh3)3Cl or Ag(PPh3)3NO3 in MeCN/CH2Cl2, respectively. Crystal data for [Et4N][(PPh3)2 {AgS2MoS2Fe}Cl2] (I): triclinic, P
(No. 2),Z=2,a=13.41(1)Å,b=15.54(1)Å,c=12.30(1)Å, =105.24(6)°, =94.63(7)°, =101.38(6)°, andV=2399(4)Å3. The bond lengths of Mo-Fe bond and the Mo-Ag distance are 2.756(2)Å and 3.033(2)Å, respectively. Crystal data for [Et4N][(PPh3)2 {AgS2WS2Fe}Cl2] (II): triclinic, P
(No. 2),Z=2,a=13.457(5))Å,b=15.601(6)Å,c=12.338(4)Å, =105.20(3)°, =94.61(4)°, =101.43(4)°, andV=2426(2)Å3. The bond length of W-Fe bond and the W-Ag distance are 2.786(2)Å and 3.076(1)Å, respectively. Crystal data for [Et4N][(PPh3)2 {CuS2WS2Fe}Cl2] (III): triclinic, P
(No. 2),Z=2,a=13.498(5)Å,b=15.372(4)Å,c=12.340(4)Å, =105.54(2)°, =93.32(3)°, =101.40(3)°, andV=2401(1)Å3. The bond lengths of W-Fe bond and the W-Cu bond are 2.800(1)Å and 2.851(1)Å, respectively. 相似文献
6.
Cp2Cr2(CO)4( - 2 - P2), 1, reacts with one molar equivalent of Fe2(CO)9 in THF to yield the mono- and di-iron complexes, Cp2Cr2(CO)4P2[Fe(CO)4], 2, (16.5% yield) and Cp2Cr2(CO)4P2[Fe(CO)4]2, 3, (16.9% yield), as dark magenta brown and dark greenish brown crystals, respectively. Both complexes were characterized by single-crystal X-ray diffraction analysis. Crystal data –2: space group =P21/c,a=17.024(1) Å,b=8.180(1) Å,c=30.891(2) Å, =100.953(5)°,V=4223.4(7)Å3,Z=8, 3743 observed reflections,R
F=0.033; 3: space group P1,a=10.209(2) Å,b=10.212(2) Å,c=15.989(3) Å, =106.93(1)°, =91.87(1)°, =119.50(1)°,V=1356.5(4) Å3,Z=2, 3489 observed reflections,R
F=0.029. 相似文献
7.
The crystal structure of the new phase Cu7(OH)6(TeO3)2(SO4)2 [a=7.389 (1),b=7.638 (1),c=7.662 (2) Å, =75.17 (1), =75.90 (1), =84.19 (1)°;Z=1] was determined by direct methods andFourier summations from X-ray intensities, and was refined in space group P
-C
i
1
toR=0.039. As usual, the Cu(II) atoms are coordinated to four O atoms forming approximately a square with average Cu-O=1.96 (3) Å; one or two more distant O neighbours complete the coordination. The shape of the TeO3 group is a rather clear-cut trigonal pyramid. A disorder was found for the SO4 tetrahedra. The compound was synthesized under hydrothermal conditions [500 (10) K, saturation vapour pressure].
Herrn Prof. Dr.K. Komarek zum 60. Geburtstag gewidmet. 相似文献
8.
Belicchi Marisa Ferrari Gasparri Giovanna Fava Pelizzi Corrado Tarasconi Pieralberto 《Transition Metal Chemistry》1985,10(8):295-299
Summary The reactions of Cu(NO3)2 · 3 H2O with 2- (2-thienyl)-1-(2-thienylmethyl)benzimidazole (L) and of CuCl2 · 2H2O with 2-(2-thienyl)benzimidazole (L) have been carried out. The crystal structure of two isolated complexes,(1) and(2), have been determined by single-crystal x-ray diffraction methods. Crystals of(1) are monoclinic, space groupP21
/c, witha=9.884(4),b=9.892(4),c=18.732(8) Å, =114.89(2)°,Z=2;R=0.068 for 1909 observed reflections. Crystals of (2) are orthorhombic, space groupPbcn, witha=14.835(1),b=8.193(1),c=20.493(1) Å,Z=4;R=0.086 for 415 observed reflections. In the complex (1) the copper co-ordination is tetragonal (compressed octahedral) and involves a nitrogen atom of the organic ligand [Cu-N 1.970(6) Å] and two oxygen atoms of the nitrate group [Cu-O 2.318(7) and 2.246(9) Å] which appears to coordinate nearly symmetrically to the metal; however it has unusually large thermal motion which suggests a fluxional behaviour. In the complex (2) the co-ordination is square planar and involves an imidazole nitrogen [Cu-N 1.95(3) Å] and a chlorine atom [Cu-Cl 2.27(1) Å]. A long interaction Cu-S=3.37(2) Å completes the co-ordination polyhedron to a very elongated distorted tetragonal bipyramid. In both compounds a thiophene ring is disordered. 相似文献
9.
U. Siemeling R. Krallmann P. Jutzi B. Neumann H. -G. Stammler 《Monatshefte für Chemie / Chemical Monthly》1994,125(5):579-586
Summary 6,6,8,8-Tetramethyl-7-oxa-6,8-disila[3]ferrocenophane2 was obtained from the di(alkoxysilyl) ferrocene (H4C5SiMe2OR)2Fe (R=CH2CH2OCH2CH2OCH2CH2OMe) by hydrolysis and subsequent intramolecular disiloxane formation. 2,2,3,3,4,4,5,5,6,6,8,8-Dodecamethyl-7-oxa-6,8-disila-[3]ferrocenophane3 was formed by air oxidation of 2,23,3,4,4,5,5,6,6,7,7-dodecamethyl-6,7-disila[2]ferrocenophane. The crystal structures of both compounds were determined by single-crystal X-ray diffraction (2:a=8.5330(10),b=15.610(3),c=18.774(5)Å, =70.68(2), =77.94(2), =75.150(10)°,V=2259.8(8)Å3,Z=6, space group P
,R=0.045,R
w
=0.044;3:a=12.388(3),b=9.924(3),c=19.136(10)Å, =105.11(3)°,V=2271.2(15)Å3,Z=4, space group P21/c,R=0.076,R
w
=0.060). Owing to the flexibility of the disiloxane bridge,2 and3 are unstrained molecules.
[3]Ferrocenophane mit Tetramethyldisiloxan-Brücke: Synthese und Molekülstruktur
Zusammenfassung 6,6,8,8-Tetramethyl-7-oxa-6,8-disila[3]-ferrocenophan2 entsteht aus dem Di(alkoxysilyl)ferrocen (H4C5SiMe2OR)2Fe (R=CH2CH2OCH2CH2OCH2CH2OMe) durch Hydrolyse und anschließende intramolekulare Disiloxan-Bildung. 2,2,3,3,4,4,5,5,6,6,8,8-Dodecamethyl-7-oxa-6,8-disila[3]ferrocenophan3 wurde durch Luftoxidation von 2,2,3,3,4,4,5,5,6,6,7,7-Dodecamethyl-6,7-disila[2]ferrocenophan erhaeten. Die Kristallstrukturen beider Verbindungen wurden durch Einkristall-Röntgenstrukturanalyse bestimmt (2:a=8.5330(10),b=15.610(3),c=18.774(5)Å, =70.68(2), =77.94(2), =75.150(10)°,V=2259.8(8)Å3,Z=6, Raumgruppe P ,R=0.045,R w =0.044;3:a=12.388(3),b=9.924(3),c=19.136(10)Å, =105.11(3)°,V=2271.2(15)Å3,Z=4, Raumgruppe P21/c,R=0.076,R w =0.060). Wegen der Flexibilität der Disiloxan-Brücke sind2 und3 ungespannte Moleküle.相似文献
10.
Filinchuk Ya. E. Davydov V. N. Mys'kiv M. G. 《Russian Journal of Coordination Chemistry》2001,27(7):505-510
Crystals of [Cu(DAF)(H2O)]BF4(I) and [Cu(DAF)(ClO4)] (II) (DAF is diallyl formamide) were synthesized by an alternate-current electrochemical method, and their structures were determined (MoK
radiation, 1247 and 859 independent reflections with I 2(I), R= 0.043 and 0.032 for Iand II, respectively). The complexes crystallize in space group P21/n, Z= 4. For I, a= 10.782(3) Å, b= 12.096(5) Å, c= 9.185(3) Å, = 103.62(3)°, and V= 1164.2(7) Å3; for II, a= 10.064(3) Å, b= 10.753(6) Å, c= 10.002(3) Å, = 87.52(4)°, and V= 1081.4(8) Å3. The copper atom in structures Iand IIcoordinates both C=C bonds in one DAF molecule and oxygen atom of the amide group of another DAF molecule, as well as an oxygen atom of H2O (in I) or ClO4(in II) in the axial position. The uncommon behavior of the anions in structures Iand IIis explained by their different values of Pierson hardness. 相似文献
11.
Nina G. Furmanova Natalya I. Sorokina Valery I. Andrianov Ursula Bologa Alexandru T. Balaban 《Structural chemistry》1991,2(7):651-654
The structure of 1-(3,5-dimethyl-2-furyl)-3-(p-tolyl)-prop-2-en-1-one, C16H16O2 is determined by single-crystal x-ray diffractometry. Crystals are triclinic,
, a=7.381(7), b=8.871(5), c=10.745(13) Å, =93.53(7), =102.25(8),=95.43(7)°, V=682(1) Å3, Z=2, dcalc=1.170 g cm–3, (Cu K)=1.54178 Å,=5.697 cm–1, M=270.30, F(000)=256, R=0.077 for 1601 unique observed reflections. The trans-geometry of the C=C double bond, thes-cis-geometry of the C=C-C=O moiety, and thes-trans arrangement of the carbonyl and furane oxygen atoms are proved. 相似文献
12.
Kaziev G. Z. Quinones Saul O. Bel'skii V. K. Zavodnik V. I. Osminkina I. V. De Ita Antonio 《Russian Journal of Coordination Chemistry》2002,28(6):384-388
Isostructural crystals of aluminum hexamolybdenocobaltate(III) and hexamolybdenocromate(III) Al[MMo6O18(OH)6] · 16H2O (M = Co(III) and Cr(III)) were studied using X-ray diffraction analysis. These compounds crystallize in the triclinic system: space group P
, Z = 1, (calcd) = 2.665 and 2.611 g/cm3, respectively. The unit cell parameters were determined: for aluminum hexamolybdenocobaltate(III), a = 6.796(1) Å, b= 11.248(2) Å, c = 11.568(2) Å; = 101.36(2)°, = 96.95(2)°, = 102.23(2)°; for aluminum hexamolybdenocromate(III), a = 6.838(1) Å, b = 11.312(2) Å, c = 11.605(2) Å; = 101.29(3)°, = 97.13(3)°, = 102.15(3)°. 相似文献
13.
Summary Crystal structures have been determined for two nickel complexes of the monodentate S-donating ligand 1-methyl imidazoline-2(3H)-thione (mimtH). The parainagnetic trans-octahedral complex, [Ni(mimtH)4Cl2], crystallises in an orthorhombic unit cell (a=12.459(1),b=13.078(1),c=15.406(1)Å, V=2510.24Å3,Z=4, space group Pbca). Final conventional R from 1848 observed data [F>4(F)] is 0.0273. The Ni–Cl distance is. 2.537(1) Å and the mean Ni–S distance is 2.479 Å.The diamagnetic complex, [Ni(mimtH)4](BF4)2, contains a distorted square-planar cation which is H-bonded. to [BF4]– anions. The complex crystallises in an orthorhombic unit cell [a=9.810(1),b=14.585(1),c=20.120(2)Å, V=2878.8Å3,Z=4, space group Pbcn]. Final conventional R from 1756 observed data [F>4(F)] is 0.0629. The average Ni–S distance is 2.216Å. 相似文献
14.
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
15.
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
16.
Noshchenko G. V. Mykhalichko B. M. Davydov V. N. 《Russian Journal of Coordination Chemistry》2004,30(5):326-331
Crystals of the HAmp[Cu9Cl8(CCCH2OH)2] cluster compound (HAmp is the 4-aminopyridinium cation (NH2–C5H4NH)+) were obtained through ac electrochemical synthesis and their structure was determined using X-ray diffraction analysis (DARCh autodiffractometer, /2 scan mode, 3435 independent reflections with F 4(F), R = 0.047). The crystals are triclinic: space group P
, a = 12.547(5) Å, b = 12.502(4) Å, c = 8.201(2) Å, = 75.93(2)°, = 82.21(3)°, = 76.05(3)°, V = 1207(2) Å3, Z = 2. Two crystallographically independent moieties –(CCCH2OH) were detected in the complex structure. Each moiety acts as a double bridging ,-ligand and binds four or five Cu(I) atoms, thus forming the [Cu4(CCCH2OH)] and [Cu8(CCCH2OH)2] clusters. The shortest Cu···Cu distance is equal to 2.337(4) Å. 相似文献
17.
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
18.
Pavlyuk A. V. Davydov V. N. Mys'kiv M. G. 《Russian Journal of Coordination Chemistry》2003,29(3):199-202
Crystals of [97N(35)]uBr2 (IV) and [97N(35)][u2Br3] (V) were prepared by ac electrochemical synthesis from uBr2, N-allylquinolinium bromide, on copper electrodes in the ethanol–benzene medium. X-ray diffraction study has shown that crystals IV and V are monoclinic: space group A21/a, a = 13.776(3) Å, b = 14.304(3) Å, c = 13.147(2) Å, = 107.90(1) Å, V = 2465(2) Å3, Z = 8 for IV and space group P21/n, a = 13.881(2) Å, b = 15.446(2) Å, c = 7.111(1) Å, = 104.64(1)°, V = 1475.0(8) Å3, Z = 4 for V. Structures IV and V are built of the N-allylquinolinium cations and different anions i.e., (CuBr2)
n-
n forming infinite chains in IV and peculiar {[CuI
4Br6]2–}
n
arranged in polymeric chains in V. In the latter case, two independent metal atoms have trigonal–pyramidal and trigonal–planar environments. In the structures of both compounds, the C=C bond of the allyl group is not involved in coordination with the Cu(I) atom. 相似文献
19.
W. Brzyska W. Wołodkiewicz Z. Rzaczyńska T. Głowiak 《Monatshefte für Chemie / Chemical Monthly》1995,126(3):285-291
Summary A new copper(II) complex of the formula [Cu(C7H3O2Cl2)2·H2O]2 crystallizes in the triclinic system (space group P
). The cell parameters area=7.267(3),b=10.687(3),c= 10.934(3) Å, =99.88(3), =96.25(3), =94.78(3)°,V=827.1(5)Å3,Z=1,D
c=1.853(1), andD
m=1.85 Mg/m3. The two copper atoms in the molecule are held together by the four carboxylate groups of the organic ligands, and each copper atom is further bonded to a water molecule, resulting in a square pyramidal geometry. The Cu-O(carboxylate) distances are in the range of 1.955(2)-1.975(2)Å, and Cu-O(water) and Cu-Cu distances are 2.166(2) and 2.605(1)Å, respectively.
Kristallstruktur von Diaquatetrakis(-2,6-dichlorobenzoato-o,o)dikupfer(II)
Zusammenfassung Ein neuer Kupfer(II)-Komplex mit der Formel [Cu(C7H3O2Cl2)2·H2O]2 kristallisiert im triklinen System (Raumgruppe P ) mit den Zellparameterna=7.267(3),b=10.678(3),c=10.934(3)Å, =99.88(3), =96.25(3), =94.78(3)°,V=827.1(5)Å3,Z=1,D c=1.853(1) undD m=1.85 Mg/m3. Die beiden Kupferatome im Molekül werden von den vier Carboxylatgruppen der organischen Liganden zusammengehalten. Jedes Kupferatom ist zusätzlich an ein Wassermolekül gebunden, woraus eine quadratisch pyramidale Geometrie resultiert. Die Cu-O(Carboxylat)-Abstände liegen in einem Bereich von 1.955(2)–1.975(2)Å; die Cu-O(Wasser)- und Cu-Cu-Abstände betragen jeweils 2.166(2) und 2.605(1)Å.相似文献
20.
Karpova E. V. Boltalin A. I. Korenev Yu. M. Zakharov M. A. Troyanov S. I. 《Russian Journal of Coordination Chemistry》2001,27(4):286-291
Compounds [Cu2(CH2FCOO)4· 2CH3CN](CH3CN) (I) and Ag3(CF3COO)3(CH3CN)2(II) were synthesized and studied by X-ray structural analysis. Crystals Iare monoclinic, space group C2/c, a= 27.854(6), b= 8.286(2), c= 19.428(4) Å, = 106.82(3)°, V= 4292(2) Å3, Z= 8, R
1= 0.0426; crystals IIare triclinic, space group
, a= 8.676(2), b= 9.819(2), c= 11.961(2) Å, = 95.27(3), = 109.59(3)°, = 104.60(3)°, V= 911.4(3) Å3, Z= 2, R
1= 0.0252. Structure Iis composed of the structural units (lanterns) typical of copper(II) carboxylates. The presence of an additional acetonitrile molecule noncoordinated by the copper atoms makes it possible to consider compound Ias a lattice clathrate. Structure IIhas no analogs among the silver carboxylates. It simultaneously contains silver atoms with coordination numbers varying from 2 to 4. 相似文献