Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 1990-1994  (17)
  • 1965-1969
  • 1992  (17)
  • Inorganic Chemistry  (15)
  • Analytical Chemistry and Spectroscopy  (2)
  • 1
    Electronic Resource
    Electronic Resource
    1,3-Addition von Aziden an Azadecaboran: 6-Azadecaboran-4,9-diyltriazene (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2025-2026 
    Details
    ISSN: 0009-2940
    Keywords: Aza-nido-decaborane(12) ; (1H-Triazen-1,3-diyl)-aza-arachno-decaborane(13) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,3-Addition of Azides to Azadecaborane: 6-Azadecaborane-4,9-diyltriazenesnido-NB9H12 (1) reacts with azides RN3 to form a coordinative B-N bond between B9 and N1 of RN3, accompanied by the α-addition of the B4-H bond of 1 to the N3 atom of RN3. The products 2a, b (R = H, CH2Ph, respectively) thus contain an azadecaborane skeleton and a five-membered unsaturated B2N3 ring with a common B-B edge. The product 2a crystallizes in the space group Pna21.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250909
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Spaltung sperriger Diarylditelluride mit Brom und Iod[1]; Strukturbestimmung an Et4N+ 2,4,6-(i-C3H7)3C6H2TeI-2 (1992)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 761-766 
    Details
    ISSN: 0009-2940
    Keywords: Tellurium compounds ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Cleavage of Bulky Diaryl Ditellurides with Bromine and Iodine; Crystal Structure of Et4N+ 2,4,6-(i-C3H7)3C6H2TeI-2Bis(2,4,6-triisopropylphenyl) ditelluride (1a), obtained from 2,4,6-triisopropylphenylmagnesium bromide with tellurium followed by oxidation with oxygen, and bis(2,4,6-tri-tert-butylphenyl) ditelluride (1b) react with equimolar amounts of bromine and iodine to provide new monomeric arenetellurenyl halides 2,4,6-R3C6H2TeX (2a, b, 3a, b: R = i-C3H7, t-C4H9; X = Br, I). Both tellurenyl iodides are thermally more stable than the corresponding bromides. Green 2,4,6-(i-C3H7)3C6H2TeI (3a) reacts with Et4N+I- to give the stable, red adduct Et4N+ 2,4,6-(i-C3H7)3C6H2TeI-2 (4a). An X-ray crystal structure determination of 4a revealed a T-shaped structure of the hypervalent aryldiiodotellurate(II) anion. Iodide-ion transfer between aryldiiodotellurate(II) and arenetellurenyl iodide is a fast process (1H-NMR time scale). 125Te-NMR data of this anion and of tellurenyl halides are compared with those of the ditellurides and of lithium benzenetellurolates (LiTeR·(THF)x).
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19921250402
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Aspects of the capillary GC analysis of all-trans- and 13-cis-acitretin (1992)
    Weinheim : Wiley-Blackwell
    Journal of High Resolution Chromatography 15 (1992), S. 637-640 
    Details
    ISSN: 0935-6304
    Keywords: Capillary GC ; On-column injection ; Plasma samples ; Retinoid analysis ; Acitretin isomers ; Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The capillary gas chromatographic (CGC) analysis of the der-matological drug trans-acitretin (NeotigasonR) and its cis metabolite is described. Separation of the methyl ester derivatives can be achieved on a 90% biscyanopropylsiloxane phase. The importance of using cold on-column injection and short, thin film capillary columns is discussed. For patients treated with the prodrug of acitretin, etretinate (TigasonR), i.e. the ethyl ester of Neotigason, three compounds have to be separated. Selectivity tuning is required for successful CGC separation. An alternative can be found in the selectivity of ion monitoring mass spectroscopy. Analysis of plasma samples involves liquid-liquid extraction, a derivatization step, and HPLC purification.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/jhrc.1240151003
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Quantification of molecular secondary ion mass spectrometry by internal standards (1992)
    Chichester : Wiley-Blackwell
    Biological Mass Spectrometry 27 (1992), S. 1148-1150 
    Details
    ISSN: 0030-493X
    Keywords: Chemistry ; Analytical Chemistry and Spectroscopy
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/oms.1210271029
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Synthese und Kristallstruktur von Hydronium-tris-ethylendiamin-cobalt(rhodium)-μ-trichloro-nonachlorotrirhenat(II)-chlorid, H3O[MEn3][Re3Cl12]Cl (M=Co, Rh) (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 607 (1992), S. 91-95 
    Details
    ISSN: 0044-2313
    Keywords: Rhenium complexes ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of Hydronium-tris-ethylenediamine-cobalt(rhodium)-μ-trichloro-nonachlorotrirhenate(III)-chloride, H3O[MEn3][Re3Cl12]Cl (M=Co, Rh)The chlorides H3O[MEn3][Re3Cl12]CI (M = Co, 1; Rh, 2) crystallize from hydrochloric acid solutions of ReCl3 and MEn3 · 3H2O as deep red hexagonal columns. They are isotypic and crystallize with the hexagonal system (P6, Z = 1; 1: a = 1010.87(3); c = 794.30(4) pm, R = 0.023, Rw = 0.016; 2: a = 1018.58(3); c = 794.74(4) pm, R = 0.026, Rw = 0.018). The anions [Re3Cl12]3- are connected via H3O+ cation (C.N. 3). The large channels that run in the [001] direction contain, alternatively, the cations [MEn3]3+ and the lonesome Cl--anions
    Notes: Die Chloride H3O[MEn3][Re3CI12]CI(M = Co, 1; Rh, 2) Kristallisieren in Form tiefroter hexagonaler Säulen aus salzsauren Lösungen von ReCI3 und MEn3CI3 · 3H2O aus. Sie sind isotyp und Kristallisieren im hexagonalen System (P6, Z = 1; 1: a = 1010,87(3); C = 794,30(4)pm, Rw = 0,016; : a = 1018,58(3); c = 794,74(4)pm, R = 0,026, Rw = 0,018). Die Anionen [ Re3Cl12]3- werden über H3O+ (C.N. 3) verknüpft; in die entstehenden Kanäle sind längs [001] abwechselnd die Kationen [MEn3]3+ und die einsamen Cl--Ionen eingelagert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926070115
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    Molekül- und Kristallstruktur von Ytterbium(III)-triaqua-trinitrat, Yb(H2O)3(NO3)3 (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 615 (1992), S. 16-18 
    Details
    ISSN: 0044-2313
    Keywords: Ytterbium nitrates ; synthesis ; crystal structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Molecular and Crystal Structure of Ytterbium(III)-triaqua-trinitrate, Yb(H2O)3(NO3)3Yb(H2O)3(NO3)3 crystallizes from a concentrated solution of Yb2O3 in nitric acid in a vacuum desiccator at ambient temperature as colourless single crystals. The crystal structure was determined from single crystal four-circle diffractometer data (R3, Z = 6, a = 1175.5(1), c = 1117.7(2) pm, Vm = 134.25 cm3/mol, R = 3.0%, Rw = 2.9%). The structure may be viewed at as a heavily compressed packing of [Yb(H2O)3(NO3)3] molecules. Yb3+ is coordinated by three bidentate nitrate ligands and three water molecules so that a tricapped trigonal prism (C.N. 9) of oxygen atoms results as the coordination polyhedron.
    Notes: Yb(H2O)3(NO3)3 kristallisiert aus einer konzentrierten Lösung von Yb2O3 in Salpetersäure im Vakuumexsikkator bei Raumtemperatur in Form farbloser Einkristalle aus. Die Kristallstruktur wurde aus Einkristall-Vierkreis-Diffraktometer-Daten bestimmt (R3, Z = 6, a = 1175,5(1), c = 1117,7(2) pm, Vm = 134,25 cm3/mol, R = 3,0%, Rw = 2,9%). Sie kann als stark gestauchte Kugelpackung von [Yb(H2O)3(NO3)3]- Molekülen aufgefaßt werden. In diesen ist Yb3+ von drei zweizähnigen Nitratliganden und drei Wassermolekülen in Form eines dreifach bekappten trigonalen Prismas (C. N. 9) von Sauerstoffatomen umgeben.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926150904
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    Synthese, Struktur und Thermolyse der ternären Ammoniumnitrate (NH4)3[M2(NO3)(9] (M = La—Gd)Professor Rudolf Hoppe zum 70. Geburtstage gewidmet (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 616 (1992), S. 141-144 
    Details
    ISSN: 0044-2313
    Keywords: Crystal structure ; Synthesis ; Thermolysis, Lanthanides ; Ternary ammonium nitrates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Structure, and Thermolysis of the (NH4)3[M2(NO3)9] (M = La—Gd)The ternary ammonium nitrates (NH4)3[M2(NO3)9] (M = La-Gd) are obtained as single crystals from a solution of the respective sesquioxides in a melt of NH4NO3 and sublimation of the excess NH4NO3. In the crystal structure of (NH4)3[Pr2(NO3)9] (cubic, P4332, Z = 4, a = 1 377.0(1) pm, R = 0.038, Rw = 0.023) Pr3+ is surrounded by six bidentate nitrate ligands of which three are bridging to neighbouring Pr3+ ions. This results in a branched folded chain, held together by the NH4+ ions which occupy cavities in the structure. (NH4)3[Pr2(NO3)9] is the first intermediate product of the thermal decomposition of (NH4)2[Pr(NO3)5(H2O)2] · 2H2O.
    Notes: Die ternären Ammoniumnitrate (NH4)3[M2(NO3)9] (M = La—Gd) erhält man in Form von Einkristallen durch Auflösen der entsprechenden Sesquioxide in einer Schmelze von NH4NO3 und Entfernen des Überschusses durch Sublimation. Die Strukturanalyse am Beispiel von (NH4)3[Pr2(NO3)9] (kubisch, P4332, Z = 4; a = 1377,0(1) pm; R = 0,038; Rw = 0,023) zeigt, daß Pr3+ von sechs zweizähnigen Nitratliganden umgeben ist, von denen drei jeweils zu einem weiteren Pr3+-Ion verbrücken. Dadurch entsteht eine verzweigte, gefaltete Kette. Sie wird durch NH4+-Ionen zusammengehalten, die sich in Hohlräumen befinden. (NH4)3[Pr2(NO3)9] stellt die erste Stufe beim thermischen Abbau von (NH4)2[Pr(NO3)9(H2O)2] · 2H2O dar.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926161021
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Cs4[La(NO3)6](NO3). HNO3: Das erste Salpetersäureaddukt eines ternären Alkali-Lanthanidnitrats (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 610 (1992), S. 20-22 
    Details
    ISSN: 0044-2313
    Keywords: Crystal structure ; lanthanides ; adducts ; complex nitrates ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Cs4[La(NO3)6](NO3) · HNO3: The First Nitric Acid Adduct of a Ternary Alkali Lanthanide NitrateIn the crystal structure of Cs4[La(NO3)6](NO3). HNO3 (monoclinic, P21/c, Z = 2, a = 787.3(2); b = 1353.0(3); c = 1141.8(7) pm; β = 94,37(3)°) La3+ has a coordination number of twelve (six bidentate nitrate ligands). The structure may be viewed at as a layer structure: Layers of the composition [Cs(1)4La2(NO3)12]2-, and [Cs(2)4(NO3)2(HNO3)2]2+ are stacked alternatively in the [100] direction.
    Notes: In der Kristallstruktur von Cs4[La(NO3)6](NO3) · HNO3 (monoklin, P21/c, Z = 2, a = 787,3(2); b = 1353,0(3); c = 1141,8(7)pm; β = 94,37(3)°) hat La3+ die Koordinationszahl zwölf (sechs zweizähnige Nitratliganden). Sie kann als Schichtstruktur aufgefaßt werden: Zwischen Schichten der Zusammensetzung [Cs(1)4La2(NO3)12]2-, die längs [100] gestapelt sind, liegen Cs(2)+- und NO3--Ionen sowie HNO3-Moleküle, die ihrerseits Schichtpakete [Cs(2)4(NO3)2(HNO3)2]2+ bilden.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926100104
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    Synthese, Kristallstruktur und thermischer Abbau von Cs1,5[Re3I3Cl7,5(H2O)1,5] (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 610 (1992), S. 15-19 
    Details
    ISSN: 0044-2313
    Keywords: Mixed ternary ReIII-halides ; synthesis ; crystal structure ; infrared spectroscopy ; thermal behaviour ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Crystal Structure and Thermal Behaviour of Cs1,5[Re3I3Cl7,5(H2O)1,5]Dark brown tetrahedra of Cs1,5[Re3I3Cl7,5(H2O)1,5] crystallize on slow cooling of a hot saturated solution of ReI3 and CsCl in conc. hydrochlorid acid. The crystal structure (cubic, P43m (No. 215), a = 1241.06(3)pm, Vm = 287.8(1) cm3mol-1, Z = 4, R = 0.067, Rw = 0.037) is built up from isolated building units [Re3I3Cl7,5(H2O)1,5]1,5- with statistical distribution of chloride ions and water molecules in the in plane, terminal positions. Consistent with the result based on the X-ray analysis, the IR-spectrum shows one band for the OH stretching frequencies of the water molecules coordinated to the Re3 triangle at 3240 cm-1. The anions are arranged in the fashion of a cubic closest packing with the cesium ions occupying all octahedral and one quarter of the tetrahedral interstices. Temperature-dependent Guinier-Simon photographs in connection with DTA/TG investigations reveal that Cs1,5[Re3I3Cl7,5(H2O)1,5] releases water at 190°C accompanied with a structural transition and the dehydration product decomposes at 370°C to Cs2ReCl6-xIx, Re3I3+yCl6-y and rhenium metal.
    Notes: Tiefdunkelbraune Tetraeder von Cs1,5[Re3I3Cl7,5(H2O)1,5] Kristallisieren beim langsamen Eindunsten einer heißen, gesättigten Lösung von ReI3 und CsCl in konz. Salzsäure. In der Kristallstruktur (kubisch, P43m (Nr. 215), a = 1241,06(3) pm, Vm = 287,8(1) cm3mol-1, Z = 4, R = 0,067, Rw = 0,037) sind isolierte Baugruppen [Re3I3Cl7,5(H2O)1,5]1,5- mit statistischer Verteilung von Chlorid-Ionen und Wassermolekülen in den in plane, terminal-Positionen strukturbestimmend. übereinstimmend mit diesem röntgenographischen Befund beobachtet man im IR-Spektrum eine Bande für die Valenzschwingungen des Koordinationswassers bei 3240 cm-1. Die Anionen sind nach dem Motiv einer kubisch-dichtesten Packung angeordnet, die Caesium-Ionen besetzen in ihr sämtliche Oktaeder- und ein Viertel der Tetraederlücken. Heiz-Guinier-Simon-Aufnahmen und DTA/TG-Untersuchungen zeigen, daß Cs1,5[Re3I3Cl7,5(H2O)1,5] bei 190°C zunächst Koordinationswasser unter Änderung der Struktur abgibt und sich bei 370°C zu Cs2ReCl6-xIx, Re3I3+yCl6-y und Rhenium zersetzt.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926100103
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Cooperative Effects in π-Ligand Bridged Dinuclear Complexes. XII [1]. Heterodinuclear Electron Poor μ-Cyclooctatetraene Complexes with CrFe-and CrCo-Combinations (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 611 (1992), S. 35-42 
    Details
    ISSN: 0044-2313
    Keywords: Heterodinuclear Cyclooctatetraene Complexes ; Synthesis ; Crystal Structure ; ESR Spectrum ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Kooperative Wirkung in π-Ligand-verbrückten Zweikernkomplexen. XII. Gemischtkernige elektronenarme μ-Cyclooctatetraen-Zweikernkomplexe mit CrFe-und CrCo-KombinationenDie synfacialen gemischtkernigen μ-Cot-Zweikernkomplexe [(CpCr)(CpM)]μ-Cot (M = Fe, 3; M = Co, 4) (Cp = Cyclopentadienyl; Cot = Cyclooctatetraen) werden in thermischen Reaktionen aus der einkernigen Sandwichverbindung CpCr(n6-Cot) und CpMLn [M = Fe, Ln = Benzol (Bz); M = Co, Ln = (C2H4)2] gebildet. 3 besitzt zwei ungepaarte Elektronen, während 4 mit nur einem ungepaarten Elektron SSR-ak-tiv ist. Aufgrund der Molekülstruktur von 3 und den ESR-Daten von 4 kann gefolgert werden, daß die ungepaarten Elektronen dieser Produkte hauptsächlich auf den Cr-Zentren lokalisiert sind. Daraus ergibt sich eine enge elektronische Verwandtschaft zwischen den hetero-dinuklearen Verbindungen 3 und 4 und den einkernigen Sandwichverbindungen Chromocen beziehungsweise CpCrBz.
    Notes: The synfacial heterodinuclear μ-Cot complexes (Cot = cyclooctatetraene) [(CpCr) (CpM)]μ-Cot (Cp = cyclopentadienyl; M = Fe, 3; M = Co, 4) are formed in a thermal reaction of the mononuclear mixed sandwich compound CpCr(n6-Cot) and CpMLn [M = Fe, Ln = benzene (Bz); M = Co, Ln = (C2H4)2]. 3 possesses two unpaired electrons whereas 4 has only one unpaired electron and is ESR active. From the molecular structure of 3 and from the ESR data of 4 it can be deduced that the unpaired electrons are localized at the Cr centers predominantly forcing a close electronical relation between the heterodinuclear compounds 3 and 4 and the mononuclear sandwich complexes chromocene and CpCrBz, respectively.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926110506
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...