1,721,108 research outputs found
MIXED GERMYLENES FROM (PENTAMETHYLCYCLOPENTADIENYL)GERMANIUM CHLORIDE AND (PENTAMETHYLCYCLOPENTADIENYL)GERMANIUM TETRAFLUOROBORATE
No full textJutzi P, HAMPEL B, HURSTHOUSE MB, HOWES AJ. MIXED GERMYLENES FROM (PENTAMETHYLCYCLOPENTADIENYL)GERMANIUM CHLORIDE AND (PENTAMETHYLCYCLOPENTADIENYL)GERMANIUM TETRAFLUOROBORATE. ORGANOMETALLICS. 1986;5(10):1944-1948
SYNTHESIS OF TRIMETHYLSILYLATED GERMANOCENES - X-RAY STRUCTURE OF AND STERIC EFFECTS IN HEXAKIS(TRIMETHYLSILYL)GERMANOCENE
No full textJutzi P, SCHLUTER E, HURSTHOUSE MB, ARIF AM, SHORT RL. SYNTHESIS OF TRIMETHYLSILYLATED GERMANOCENES - X-RAY STRUCTURE OF AND STERIC EFFECTS IN HEXAKIS(TRIMETHYLSILYL)GERMANOCENE. JOURNAL OF ORGANOMETALLIC CHEMISTRY. 1986;299(3):285-295
meso-octacyclopropylcalix[4]pyrrole ethanol solvate
No full textThe title compound, C44H52N4.C2H5OH, is a calix[4]pyrrole-type macrocycle acting as a receptor, by means of hydrogen-bond interactions to an ethanol solvent. The pyrrole groups are arranged in a 1,3-alternate conformation which gives rise to disorder in the ethanol guest, due to its ability to coordinate both above and below the plane of the macrocycle
TRANSITION-METAL COMPLEXES OF CYCLOPENTADIENYLGERMYLENES - THE X-RAY STRUCTURE OF (ME5C5)[(ME3SI)2CH]GE-]W(CO)5
No full textJutzi P, HAMPEL B, HURSTHOUSE MB, HOWES AJ. TRANSITION-METAL COMPLEXES OF CYCLOPENTADIENYLGERMYLENES - THE X-RAY STRUCTURE OF (ME5C5)[(ME3SI)2CH]GE-]W(CO)5. JOURNAL OF ORGANOMETALLIC CHEMISTRY. 1986;299(1):19-27
PENTA(METHOXYCARBONYL)CYCLOPENTADIENYL-SUBSTITUTED GERMANIUM(II) AND TIN(II) COMPOUNDS - X-RAY CRYSTAL-STRUCTURE OF BIS[PENTA(METHOXYCARBONYL)CYCLOPENTADIENYL]TIN(II)
No full textJutzi P, KOHL FX, SCHLUTER E, HURSTHOUSE MB, WALKER NPC. PENTA(METHOXYCARBONYL)CYCLOPENTADIENYL-SUBSTITUTED GERMANIUM(II) AND TIN(II) COMPOUNDS - X-RAY CRYSTAL-STRUCTURE OF BIS[PENTA(METHOXYCARBONYL)CYCLOPENTADIENYL]TIN(II). JOURNAL OF ORGANOMETALLIC CHEMISTRY. 1984;271(1-3):393-402
DERIVATIVES OF [RH6(CO)13C]2- - SOLUTION STRUCTURE OF [RH6H(CO)13C]-FROM NUCLEAR MAGNETIC-RESONANCE MEASUREMENTS AND THE X-RAY CRYSTAL-STRUCTURE OF [RH6(CO)11C(MU-PH2PCH2CH2PPH2)]2-
No full textDERIVATIVES OF [RH6(CO)13C]2- - SOLUTION STRUCTUR
Synthesis, structure, and isomerisation of triruthenium and triosmium clusters derived from 3-dimethylaminoprop-1-yne; X-ray crystal structure of [Ru3 -H(CO)9(Me2N+=C-C=CH2)]
No full textNMR and X-ray Structural Characterization of a Cisplatin Analogous Able to Slow Down the Pt-N7 Rotation of a Coordinated Guanine Base by a Billion Times: the 2,2'-Bipiperidine(dimethylmalonato)platinum(II) Complex
No full textCRYSTALLINE TL2B2H9C2ME2 - SYNTHESIS AND SOLID-STATE STRUCTURE - A CONTRIBUTION TO THE PROBLEM OF TL(I)-TL(I) INTERACTIONS
No full textJutzi P, WEGENER D, HURSTHOUSE MB. CRYSTALLINE TL2B2H9C2ME2 - SYNTHESIS AND SOLID-STATE STRUCTURE - A CONTRIBUTION TO THE PROBLEM OF TL(I)-TL(I) INTERACTIONS. CHEMISCHE BERICHTE. 1991;124(2):295-299.Crystalline Tl2B9H9C2Me2 (1) is obtained in the reaction of the carborane B9H11C2Me2 with two equivalents of thallium(I) ethanolate. An X-ray diffraction study of 1 shows - contrary to the expectation - the presence of isolated thallium ions and thalladicarbollide counteranions. The latter represent ion pairs composed of Tl(I)+ and B9H9C2Me2 inverted left perpendicular 2- units forming slipped icosahedrons. All possible Tl-Tl distances in 1 are too long for even weak attractive interactions, with one exception: A set of symmetry-equivalent cations possesses a Tl-Tl distance of 3.67 angstrom, which is in a range postulated by calculations for weak bonding
Predictable and unpredictable reactions between 4,4′-dipyridyldisulfide and phosphonodithioato/dithiophosphato NiII complexes: novel coordination polymers and the unique example of 4,4′-dipyridyltrisulfide
No full textThe reactions between dpds and the phosphonodithioato and dithiophosphato NiII complexes [Ni(MeOpdt)2] (1), [Ni(EtOpdt)2] (2), and [Ni((EtO)2PS2)2] (3) yielded the novel coordination polymers (1·dpds)∞, (2·dpts)∞, and (3·dps)∞, featuring three different spacers ensuing from in situ chemical rearrangement of the starting dpds reagent (dpds, 4,4′-dipyridyldisulfide; dps, 4,4′-dipyridylmonosulfide; dpts, 4,4′-dipyridyltrisulfide)
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