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  • Inorganic Chemistry  (23)
  • Computational Chemistry and Molecular Modeling
  • 1985-1989  (22)
  • 1930-1934  (2)
  • 1987  (14)
  • 1986  (8)
  • 1932  (1)
  • 1931  (1)
Collection
Publisher
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  • 1985-1989  (22)
  • 1930-1934  (2)
Year
  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 32 (1987), S. 457-468 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: With this work, we begin our treatment of the transition metal electron affinities. A procedure, REDUCE, for reducing the number of parental couplings per configuration present in the first order wave function from as many as 100 to only a few is introduced. Progress toward a comprehensive relativistic-correlation theory is discussed. Several states in Sc- were examined but none were found to be bound. Two new bound states were obtained for Cu-: 3d9 4s 4p2 5D and 3d8 4s 4P3 7F0, with electron affinities 0.109 and 1.052 eV, respectively.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 889-893 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The nucleophilic substitution of chloride in dichlorocyclobutenedione by carbonylmetallates gives the μ-(3,4-dioxo-1-cyclobutene-1,2-diyl) complexes LnM(C4O2)MLn 1 [MLn=Re(CO)5, Mn(CO)5, W(CO)3(η5-C5H5)] and the μ-(2-chloro-3,4-dioxo-1-cyclobuten-1-yl) complexes LnM— [MLn = Mn(Co)5, W(CO)3(η5-C5H5), Mo(CO)3(η5-C5H5)], respectively. The structure of the dirhenium complex (OC)5Re(C4O2)Re(CO)5 (1a) was determined by X-ray diffraction. The Re-C bonds are slightly shortened with respect to single bonds, Re-C=2.18(1)/2.17(1)Å [monoclinic, P21, a=7.031(1), b=11.532(1), c=11.418(1)Å, β=105.54(1)°, V=891.95Å3, dcalc=2.727 g/cm3 for Z=2, Rw=0.031 for 252 refined parameters and 3539 observables with I ≥ 2.0σ(I)].
    Notes: Die nucleophile Substitution von Chlorid in Dichlorcyclobutendion durch Carbonylmetallate liefert die μ-(3,4-Dioxo-1-cyclobuten-1,2-diyl)-Komplexe LnM(C4O2)MLn 1 [MLn=Re(CO)5, Mn(CO)5, W(CO)3(η5-C5H5)] bzw. die μ-(2-Chlor-3,4-dioxo-1-cyclobuten-1-yl)-Komplexe LnM— [MLn = Mn(Co)5, W(CO)3(η5-C5H5), Mo(CO)3(η5-C5H5)]. Nach der Röntgenstrukturanalyse des Dirhenium-Komplexes (OC)5Re-(C4O2)Re(CO)5 (1a) sind die Re-C-Bindungen gegenüber Einfachbindungen leicht verkürzt, Re-C=2.18(1)/2.17(1)Å [monoklin, P21, a=7.031(1), b=11.532(1), c=11.418(1)Å, β=105.54(1)°, V=891.95Å3, dber=2.727 g/cm3, Z=2, Rw=0.031 für 252 verfeinerte Parameter und 3539 Observablen mit I ≥ 2.0σ(I)].
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 895-900 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: (OC)5ReFBF3 reacts with ethyl thiocyanate, malononitrile, cyanamide, and dicyandiamide (L) to give the ionic complexes [(OC)5ReL]+BF-4 (1). Two or three Re(CO)-3 cations, respectively, can be added to tetracyanoethene and tetracyano-p-quinodimethane (TCNQ) to give 2, 3. With the anions of tricyanoethenolate, TCNQ-, tricyanomethanide and dicyanamide (L-) the neutral compounds (OC)5ReL (4-7) are formed. The IR spectra and the X-ray structure analyses of [(OC)5Re(NCNC(NH2)2]+BF -4 (1d), (OC)5ReNCC(CN)2 (6), and of (OC)5ReNCNCN (7) show that the ligands are coordinated in all cases via the nitrile N-atom to the metal.
    Notes: (OC)5ReFBF3 setzt mit Ethylthiocyanat, Malononitril, Cyanamid und Dicyandiamid (L) zu den ionogenen Verbindungen [(OC)5ReL]+BF-4 (1) um. An Tetracyanethen sowie an Tetracyan-p-chinodimethan lassen sich zwei bzw. drei Re(CO)-3-Kationen unter Bildung von 2 und 3 addieren. Mit den Anionen Tricyanethenolat, TCNQ-, Tricyanmethanid und Dicyanamid (L-) entstehen die Neutral-Komplexe (OC)5ReL (4-7). Die IR-Spektren sowie die Röntgenstrukturanalysen von [(OC)5Re(NCNC(NH2)2]+BF -4 (1d), (OC)5ReNCC(CN)2 (6) und (OC)5ReNCNCN (7) zeigen, daß die Liganden in allen Fällen über das Nitril-N-Atom an das Metall koordiniert sind.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 253-254 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of the 16-electron system Re(CO)+5 [as (OC)5ReFBF3] to acetylpentacarbonylchromate and -tungstate (as NMe+4[M(CO)5C(Me)O]-, M=Cr, W) leads to the acetyl-bridged complexes (OC)5M-C(Me)-O-Re(CO)5 (1a,b). This reaction is analogous to the classic synthesis of Fischer carbene complexes from acylcarbonylmetallates and oxonium salts and provides a further example for the isolobal concept. The chromium compound 1a has been characterized by single crystal X-ray diffraction analysis.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 120 (1987), S. 1679-1682 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Anodic Oxidation of Cycloaliphatic Mono- and Diethers in Aqueous ElectrolytesThe anodic oxidation of cycloaliphatic ethers such as tetrahydrofuran5) and tetrahydro-2H-pyran (1) as well as cycloaliphatic diethers such as 1,4-dioxane (3) and 1,3-dioxolane (6) was investigated under various conditions in aqueous 1 M H2SO4. The primary products in all cases are those of anodic hydroxylation in the 2-position to yield cyclic hemiacetals. This oxidation gives with platinum current efficiencies which are much larger than the results of the anodic methoxylation in methanol. The high selectivity in some cases is explained in terms of an O-insertion from PtO2. - The follow-up oxidation leads in the case of the cyclic monoethers to lactones, predominantly with lead dioxide. δ-Valerolactone is synthesized with more than 60% current efficiency from 1. With diethers 3 and 6, anodic products of ring fragmentation are formed. The product distribution is indicative of an O-insertion under ring expansion.
    Notes: Die anodische Oxidation cycloaliphatischer Ether wie Tetrahydrofuran5) und Tetrahydro-2H-pyran (1) sowie cycloaliphatischer Diether wie 1,4-Dioxan (3) und 1,3-Dioxolan (6) wurde unter verschiedenen Elektrolysebedingungen in wäßriger 1 M H2SO4 untersucht. Übereinstimmend wird primär durch anodische Hydroxylierung in 2-Stellung ein cyclisches Halbacetal gebildet. An Platin sind die Stromausbeuten viel höher als bei der analogen Methoxylierung in Methanol. Die teilweise erreichte hohe Selektivität wird auf eine spezifische O-Insertion aus PtO2 zurückgeführt. - Die Weiteroxidation führt bei den cyclischen Monoethern, vor allem an Bleidioxid, zum Lacton. Aus 1 entsteht mit über 60% Stromausbeute das δ-Valerolacton. Im Fall der Diether 3 und 6 bilden sich Produkte der anodischen Ringfragmentierung; das Produktspektrum ist indikativ für eine O-Insertion unter Ringerweiterung.
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  • 6
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Azo Bridges from Azines, VII1). - Diels-Alder Reactions with Inverse Electron Demand between Isopyrazoles add Cycloalkenes or Cycloalkadienes. - A Comparison of Acid Catalysis and Acceleration by PressureThe acid-catalysed reaction of the isopyrazoles 1 and 2 with the cycloalkenes 3-8, norbornene (9), 1,4-cyclohexadiene (18), 1,5-cyclooctadiene (19), norbornadiene (20), and benzonorbornadiene (21) yields the expected azo-bridged cycloadducts 10-17 and 22-27. From 19 are also obtained the bisadducts 24a and 24b. At higher pressure (7 kbar) the non-acid-catalysed reaction of 2 and the previously mentioned olefines produces the respective cycloadducts usually in higher yields. In the case of 20 the additional bisadducts exo,exo-26b and endo,exo-26b are formed. Reaction rates for the (pressure-controlled) cycloadditions correlate with the reaction enthalpies of the cycloaddition between cycloalkenes and 1,3-cyclopentadiene. The exo/endo ratio of cycloadducts 25b, formed from 2 and 20 proves to be independent of temperature and pressure.
    Notes: Die Isopyrazole 1 und 2 liefern unter Säurekatalyse mit den C3—C8-Cycloalkenen (3-8) sowie mit Norbornen (9), 1,4-Cyclohexadien (18), 1,5-Cyclooctadien (19), Norbornadien (20) und Benzonorbornadien (21) die erwarteten Cycloaddukte 10-17 und 22-27 mit Azobrücke. Mit 19 entstehen dabei auch die Bisaddukte 24a und 24b. Ohne Säurekatalyse bilden sich aus 2 und den Olefinen die entsprechenden Cycloaddukte unter 7 kbar Druck meist in höherer Ausbeute, mit 20 zusätzlich die Bisaddukte exo,exo-26b und endo,exo-26b. Die unterschiedlichen Reaktionsgeschwindigkeiten der Cycloalkene bei Reaktionen unter Druck korrelieren mit den Reaktionsenthalpien für die Addition von 1,3-Cyclopentadien. Das exo/endo-Verhältnis der Cyclo-addukte 25b aus 2b + 20 erweist sich druck- und temperatur-unabhängig.
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  • 7
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes of Functional Isocyanides, XVI1). - 1,3-Dipolar Cycloadditions of heteroallenes to the Organometallic Nitrile Ylides [(OC)5M—C≡N—CHR]- (M = Cr, W; R = CO2Et)In the presence of bases (NEt3, KtBuO, LinBu), the isocyanoacetic ester ligand in M(CO)5CNCH2CO2Et (M = Cr, W, 2,3) reacts with the heteroallenes PhN=C=O and PhN=C=S regio- and site-selectively to give the carbenoid heterocyclic ligands {:CN(H)-C(CO2Et)C(X-)NPh }- (X = O, S; 6,7, 13, 14). The exocyclic olate and thiolate functions have been alkylated and acylated (8-10, 15), while the latter has also been oxidized to give the disulfide 16. [M{CN(H)C(CO2Et)C(S-)NPh }(CO)5]- (M = Cr, W), moreover, has been introduced into the platinum complexes PtCl2(PEt3)2 and [PtCl(PPh3)2]2(BF4)2 where it acts as a monodentate ligand coordinating with its exo-sulfur atom (17-19). The structural assignments are made on the basis of IR, NMR (1H, 13C, 31P) and mass spectroscopy data as well as of an X-ray structure analysis of NEt3H-[W {CN(H)C(CO2Et)C(O-NPh }(CO)5] (7). In the solid state strong hydrogen bonding occurs both between the and the exocyclic olate function of the anion, and between the NH and O=C(ester) groups of two complexes with formation of almost discrete dimers.
    Notes: Der Isocyanessigester-Ligand in M(CO)5CNCH2CO2Et (M = Cr, W, 2,3) reagiert in Gegenwart von Basen (NEt3, KtBuO, LinBu) mit den Heteroallenen PhN=C=O und PhN=C=S regio- und seitenselektiv zu den carbenoiden Heterocyclenliganden {:CN(H)-C(CO2Et)C(X-)NPh }- (X = O, S; 6,7, 13, 14). Die exocylischen Olat- und Thiolatfunktionen lassen sich alkylieren und acylieren (8-10, 15) bzw. zum Disulfid 16 oxidieren. Darüber hinaus wird [M{CN(H)C(CO2ET)C(S-)NPh }C(CO)5]- (M = Cr, W) als einzähniger, über das exo-Schwefelatom koordinierender Ligand in die Platinkomplexe PtCl2(PEt3)2 und [PtCl(PPh3)2]2(BF4)2 eingebaut (17-19). Die Strukturzuweisungen erfolgen auf der Basis von IR-, Kernresonanz (1H, 13C, 31P)- und massenspektroskopischen Daten, sowie der Röntgenstrukturanalyse von NEt3H-[W{CN(H)C(CO2Et)C(O-)NPh }(CO)5] (7). Im Festkörper liegen starke H-Brücken sowohl zwischen Kation und exocyclischer Olat-Funktion des Anions, als auch zwischen den NH- und O=C(Ester)-Gruppierungen je zweier Komplexanionen vor, so daß nahezu diskrete Dimere resultieren.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 119 (1986), S. 1217-1231 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Tetrathiosquarate, C4S42-, a Versatile Ligand in Metal Complexes, II1)Tetrathiosquarate acts as bridging bis(chelate) ligand in the complexes (PPh3)2MC4S4M-(PPh3)2 (M = Cu, Ag, Rh) (1a, b, d), Ph3PAuC4S4AuPPh3 (1c), [(Et3P)2PtC4S4Pt(PEt3)2]2+ (Cl-)2 (1e), [Cl2PdC4S4PdCl2]2- (AsPh4+)2 (1f), [(Ph3P)2PtC4S4Pt(PPh3)2]2- (AsPh4+)2 (1g), and in Me2AuC4S4AuMe2 (1h), as monochelate in (Ph2PCH2CH2PPh2)NiC4S4 (2) [C4S4Ni(py)2 C4S4]2- (AsPh4+)2·2 Pyridin (3) and [C4S4ZnC4S4]2- (AsPh4+)2. On the basis of the bond lengths obtained by an X-ray structure analysis the ligand in 3 can be formulated as dithioxocyclobutenedithiolate. Polymeric complexes presumably with chain structure of approximate composition (M2C4S4)n (M1 = Cu, Ag, Au) and (MC4S4)n (MII = Cu, Zn, Cd, Hg, Fe, Co, Ni, Pd, Pt, Sn, Pb) precipitate from aqueous solutions of K2C4S4 and metal salts. Oligomeric complexes [C4S4MC4S4MC4S4]2- (AsPh4+)2 (7) (M = Mn, Fe, Co, Ni) and [Cun(C4S4)n+1]2- (AsPh4+)2 (9) (n = 3, 11) have been obtained from nonaqueous solutions using (AsPh4)2C4S4. [C4S4GePh3]-K+ (10), {C4S4[Co(biacetyl dioximate)2 pyridine]2} (11), {C4S4[Co(biacetyl dioximate)2PPh3]4}2+ (Cl-)2 (12), and [Mo(C4S4)Mo]4- (AsPh4+)4 (13) are complexes with C4S42- as one-, two- or fourfold monodentate ligand, respectively.
    Notes: Tetrathioquadratat tritt in den Komplexen (Ph3P)2MC4S4M(PPh3)2 (M = Cu, Ag, Rh) (1a, b, d), Ph3Ph3PAuC4S4AuPPh3 (1c), [(Et3P)2PtC4S4Pt(PEt3)2]2+ (Cl-)2 (1e), [Cl2PdC4S4PdCl2]2- (AsPh4+)2 (1f), [(Ph3P)2PtC4S4Pt(PPh3)2]2- (AsPh4+)2 (1g) sowie in Me2AuC4S4AuMe2 (1h) als verbrückender Bis(chelat)-Ligand auf. Als Monochelat-Ligand wird C4S42- in (Ph2PCH2-CH2PPh2)NiC4S4 (2), [C4S4Ni(py)2C4S4]2- (AsPh4+)2·2 Pyridin (3) und [C4S4ZnC4S4]2- (AsPh4+)2 (4) gefunden. Nach den durch Röntgenstrukturanalyse ermittelten Abständen läßt sich der Ligand in 3 als Dithioxocyclobutendithiolat formulieren. Polymere Verbindungen der ungefähren Zusammensetzung (M2C4S4)n (MI = Cu, Ag, Au) und (MC4S4)n (MII = Cu, Zn, Cd, Hg, Fe, Co, Ni, Pd, Pt, Sn, Pb) mit vermutlicher Kettenstruktur entstehen aus K2C4S4 und den Metallsalzen in wäßriger Lösung. Oligomere Komplexe definierter Zusammensetzung [C4S4MC4S4MC4S4]2- (AsPh4+)2 (7) (M = Mn, Fe, Co, Ni) und [Cun-(C4S4)n+1]2- (AsPh4+)2 (9) (n = 3, 11) wurden mit (AsPh4)2C4S4 in nicht-wäßrigem Medium erhalten. (C4S4GePh3)-K+ (10), {C4S4[Co(biacetyldioximat)2Pyridin]2} (11), {C4S4[Co(biacetyldioximat)2PPh3]4}2+ (Cl-)2 (12) und [Mo(C4S4)4Mo]4- (AsPh4+)4 (13) sind Komplexe mit C4S42- als ein-, zwei- bzw. vierfach einzähliger Ligand.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 119 (1986), S. 554-562 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photoelectron Spectroscopic Investigation of Hexahydro-1,3,5-triazinesThe PE spectra of the 1,3,5-trialkylhexahydro-1,3,5-triazines 1 - 4, of tri-1-pyrroline (5), α-tripiperideine (6), hexamethyltriisopyrazole (7) and of tri-4,5-dihydropyridazine (8) or those of their decomposition products have been obtained and interpreted with respect to the electronic structure and the conformation of the compounds. The spectra of 1 - 6 are consistent with a diequatorial-monoaxial arrangement of the nitrogen substituents in the hexahydro-1,3,5-triazine ring. 7 probably has a monoequatorial-diaxial conformation. The spectrum obtained from 8 is not in accord with the presence of the trimeric form in the gas phase.
    Notes: Die PE-Spektren der 1,3,5-Trialkylhexahydro-1,3,5-triazine 1 - 4, des Tri-1-pyrrolins (5), des α-Tripiperideins (6), des Hexamethyltriisopyrazols (7) und des Tri-4,5-dihydropyridazins (8) sowie diejenigen einiger Zerfallsprodukte wurden aufgenommen und hinsichtlich der elektronischen Struktur und der Konformation der Verbindungen ausgewertet. Die PE-Spektren von 1 - 6 stehen mit einer diäquatorial-monoaxialen, dasjenige von 7 mit einer monoäquatorial-diaxialen Stellung der Stickstoffsubstituenten am Hexahydro-1,3,5-triazin-Ring im Einklang. Das von 8 erhaltene Spektrum spricht gegen das Vorliegen dieser Verbindung in trimerer Form in der Gasphase.
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  • 10
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Photoelektronen- und UV-spektroskopische Untersuchungen zur Homokonjugation zwischen parallelen C=C- und N=N-BindungenDie Photoelektronen- und UV-Spektren von Diazaisodrinen 4 und 5 wurden gemessen und analysiert. Die beträchtliche Homokonjugation zwischen C=C- und N=N-Bindungen spiegelt sich in einem deutlich destabilisierten π-Orbital vom Norbornentyp wider. Die UV-Spektren wurden mit Hilfe der CNDO-CI-Methode interpretiert, und es ergab sich eine ausgezeichnete Übereinstimmung zwischen beobachteten und berechneten Werten. Der transanulare π- →+*-Übergang, der im Stammkohlenwasserstoff nicht erkennbar ist, läßt sich im Diazaderivat leicht identifizieren. Röntgenstrukturanalysen von 4a und 5a bestätigen im wesentlichen die durch semiempirische Methoden erhaltenen Strukturvorschläge.
    Notes: The photoelectron and UV spectra of diazaisodrin systems 4 and 5 have been measured and analyzed. The strong homoconjugative interaction between the C=C and N=N bond is reflected in a particular destabilized position of the norbornene type π orbital. The UV spectra have been assigned using a CNDO-CI treatment and excellent agreement between observed and calculated values has been achieved. The transanular π- →+* transition which is not discernible in the parent hydrocarbon can easily be identified in the diaza derivative. X-ray structure determination of 4a and 5a confirms the conclusions arrived at by semiempirical calculations.
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