ALBERT

All Library Books, journals and Electronic Records Telegrafenberg

feed icon rss

Your email was sent successfully. Check your inbox.

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

Proceed reservation?

Export
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 3615-3618 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Addition of Nucleophiles to Cyclopentadienyl(cyclohexadienyl)cobalt CationCyclopentadienyl(cyclohexadienyl)cobalt salts [Co(C5H5) (C6H7)]X (X = I, PF6) at room temperature readily add nucleophiles to form 5-exo-substituted derivatives of cyclopenta-dienyl(cyclohexadiene)cobalt Co(C5H5)(C6H7Y)(Y = CH(CO2CH3)2, N(CH3)2, N[C2H4]2O, OCH3).
    Notes: Cyclopentadienyl-cyclohexadienyl-kobalt-Salze [Co(C5H5)(C6H7)]X (X = J, PF6) addieren bei Raumtemperatur Nucleophile unter Bildung von 5-exo-substituierten Derivaten des Cyclopentadienyl-cyclohexadien-kobalts Co(C5H5)(C6H7Y) (Y = CH(CO2CH3(2) N(CH3)2, N[C2H4]2O, OCH3).
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 3780-3785 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Borabenzene Derivatives, V. Iron Complexes of 1-Phenylborinate and 1-Methylborinate IonsBy reaction of bis(borinato)cobalt complexes, Co(C5H5B-R)2 (R=C6H5, CH3), with iron carbonyles bis(borinato)diiron tetracarbonyl complexes, [Fe(CO)2(C5H5B-R)]2 (R=C6H5, CH3), are obtained for which in the solid state a doubly CO-bridged cis-structure is proposed. Pyrolysis of these compounds at 230°C yields the corresponding bis(borinato)iron derivatives, Fe(C5H5B-R)2.
    Notes: Durch Umsetzung von Bis(borinato)kobalt-Komplexen, Co(C5H5B-R)2 (R=C6H5, CH3) mit Eisencarbonylen werden Bis(borinato)dieisentetracarbonyl-Komplexe, [Fe(CO)2(C5H5-B-R)]2 (R=C6H5, CH3), erhalten, für die im festen Zustand eine doppelte CO-verbrückte cis-Struktur vorgeschlagen wird. Pyrolyse dieser Verbindungen bei 230°C ergibt die entsprechenden Bis(borinato)eisen-Derivate, Fe(C5H5B-R)2.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Borabenzene Derivatives, VIII: A New Route to Alkalimetal Borinates. Syntheses of Ruthenium, Osmium, Rhodium, and Platinum Compounds with Borinate LigandsDegradation of bis(borinato)cobalt complexes Co(C5H5B — R)2(R = C6H5, CH3) with alkalimetal cyanides MCN (M = Na, K) yields alkalimetal borinates M[C5H5B — R]. These are versatile synthetic intermediates as demonstrated by the syntheses of Ru(C5H5B — R)2 (R = C6H5, CH3), Os(C5H5B — C6H5)2, Rh(1,5-C8H12)(C5H5B — R), and Pt(CH3)3(C5H5B — C6H5).
    Notes: Der Abbau von Bis(borinato)kobalt-Komplexen Co(C5H5B — R)2 (R = C6H5, CH3) mit Alkalimetallcyaniden MCN (M = Na, K) liefert Alkalimetallborinate M[C5H5B — R]. Diese sind vielseitige Synthesezwischenprodukte, wie mit der Darstellung von Ru (C5H5B — R)2 (R = C6H5,CH3), Os(C5H5B — C6H5)2, Rh(1,5-C8H12)(C5H5B — R) und Pt(CH3)3((C5H5B — C6H5) gezeigt wird.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 1171-1174 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: (η-1,5-Cyclooctadiene)(1-4-η-1-phenyl-1-borato-1,3-cycloheptadiene)rhodium - a Complex with a Novel B-C LigandThe title complex 6 which represents the first example of the novel 1-4-η-1-borato-1,3-butadiene type structure is obtained by reaction of 1-phenyl-4,5-dihydro-1H-borepin with LiC(CH3)3 and [Rh(1,5-C8H12)Cl]2. The constitution of this 16-electron complex and the presence of a rhodiumboron bond is proved by spectroscopic methods.
    Notes: Der Titelkomplex 6, welcher das erste Beispiel des neuartigen 1-4-η-1-Borato-1,3-butadien-Strukturtyps darstellt, wird durch Umsetzung von 1-Phenyl-4,5-dihydro-1H-borepin mit LiC(CH3)3 und [Rh(1,5-C8H12)Cl]2 erhalten. Die Konstitution dieses 16-Elektronen-Komplexes und das Vorliegen einer Bor-Rhodium-Bindung wird mit spektroskopischen Methoden bewiesen.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 112 (1979), S. 607-624 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Borabenzene Derivatives, XIII. Cationic Borinato-metal Complexes. Nucleophilic Addition and Ring Contraction ReactionsSyntheses of cationic borabenzene complexes [ML(C5H5B—C6H5)]+ with ML = Co(C5H5) (1+ ), Co(C5H5B—C6H5) (2 + ), Rh{C5(CH3)5} (3 + ), Ir{C5(CH3)5} (4 + ), and Ru(C6H6) (5 +) are described. These cations are much more electrophilic than the corresponding cyclopentadienyl complexes [ML(C5H5)] +. With nucleophiles three types of reactions are observed: i) nucleophilic addition at boron producing stable adducts, e.g. in the systems l +/C5H5N,3+/CN-. and 4 + /CN-.  -  ii) ring-contraction of borinato ligands in l +,2+, and 3+ forming cyclopentadienyl ligands.  -  iii) nucleophilic addition at carbon if the nucleophile is H- (from NaBH4) producing complexes ML(4-H—C5H5B-C6H5), ML(6-H—C5H5B—C6H5), and M(LH)(C5H5B—C6H5) from 1+, 2+, and 3+.
    Notes: Synthesen kationischer Borabenzol-Komplexe [ML(C5H5B—C6H5]+ mit ML = Co(C5H5) (1+), Co(C5H5B-C6H5)(2+), Rh{C5(CH3)5} (3 + ), Ir{C5(CH3)5}(4+) und Ru(C6H6)(5+) werden beschrieben. Diese Kationen sind sehr viel elektrophiler als die entsprechenden Cyclopentadienyl-Komplexe [ML(C5H5)] +. Mit Nucleophilen werden drei Arten von Reaktionen beobachtet: 1. nucleophile Addition am Bor unter Bildung stabiler Addukte, z. B. in den Systemen 1+/C5H5N, 3+/CN- und 4+/CN-.  -  2. Ringkontraktionen von Borinat-Liganden in 1+, 2+ und 3+ unter Bildung von Cyclopentadienyl-Liganden.  -  3. nucleophile Addition am Kohlenstoff, wenn das Nucleophil H- (aus NaBH4) ist, unter Bildung von Komplexen ML(4-H—C5H5B—C6H5), ML(6-H—C5H5B—C6H5) und M(LH)(C5H5B—C6H5) aus 1+ 2+ und 3 +.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 6
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Acetylene Complexes of Molybdenocene: Synthesis via Ligand Substitution Reactions of Bis(η5-cyclopentadienyl)[(Z)-stilbene]molybdenum, a Molybdenocene Derivative with Substitution-labile OlefinThe reinvestigation of the reaction of molybdenocene dihydride, Mo(C5H5)2H2 (1), with diphenylacetylene led to the isolation and characterization of the (Z)-stilbene complex of molybdenocene, Mo(C5H5)2[(Z)-C6H5CH=CHC6H5] (3). The olefin ligand in this complex is found to be rather labile and substitution reactions with various substituted acetylenes RC≡CR′ readily gave the acetylene complexes of molybdenocene, Mo(C5H5)2(RC≡CR′) (2f-cm). The effect of the acetylene substituents R and R′ in these compounds is discussed in terms of their electronic properties.
    Notes: Bei der Wiederholung der Reaktion von Molybdänocendihydrid, Mo(C5H5)2H2 (1), mit Diphenylacetylen konnte das (Z)-Stilben-Addukt des Molybdänocens, Mo(C5H5)2[(Z)-C6H5CH=CHC6H5] (3), isoliert und charakterisiert werden. Der olefinische Ligand in 3 erweist sich als substitutionslabil: Verschiedene substituierte Acetylene RC≡CR′ reagieren mit 3 glatt zu den Acetylen-Komplexen 2f-m des Molybdänocens, Mo(C5H5)2(RC≡CR′). Der Einfluß der Acetylensubstituenten R und R′ in dieser Verbindungsklasse wird im Hinblick auf ihre elektronischen Eigenschaften untersucht.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 45-47 
    ISSN: 0009-2940
    Keywords: Diboration / Cage compound ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Catalyzed Dimerisation of 1,2-Bis(dimethylamino)-1,2-dibora-4-cyclohexene1,2-Bis(dimethylamino)-1,2-dibora-4-cyclohexene (1) dimerizes under the catalytic action of Et2O-BF3 to form the cage compound 3,7,9,11-tetrakis(dimethylamino)-3,7,9,11-tetraboratricyclo[4.2.2.22.5] dodecane (2). The crystals of 2 are triclinic, and the molecule exhibits crystallographic centrosymmetry.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2663-2666 
    ISSN: 0009-2940
    Keywords: Niobium complexes ; Methylcyclopentadienyl derivatives ; Cyclooctatetraene derivatives ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: New Cyclooctatetraene Complexes of Niobium[1]The (butadiene)niobium complexes Cp′Nb(C4H6)2 and Cp′Nb(C4H6)(PMe3)2 (Cp′=C5H4Me) react with cyclooctatetraene (COT) to give Cp′Nb(C4H6)(COT) (2), Cp′Nb(COT)2 (3), and Cp′Nb(PMe3)2(COT) (5) with fluxional COT ligands. The structure of 3 exhibits a prone-η3- and a supine-η4-COT ligand which interchange their role at elevated temperature. That of 5 shows a supine η3-COT ligand.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 23-29 
    ISSN: 0009-2940
    Keywords: Diboracycloalkanes ; Diboracycloalkenes ; Trimethylenemethane, borylation of the dianion of ; Allylboranes, B - C bond length ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses of New Organoboron Rings with two Boron Atoms by Borylation of the Trimethylenemethane DianionBorylation of Li2[C(CH2)3] (1) provides a versatile starting point for the synthesis of 5-, 6-, 7-, and 8-membered ring systems with two boron atoms and leads to 1,5-bis(dialkylamino)-3,7-dimethylene-1,5-diboracyclooctanes 2a, b (a: R=Et; b: R=iPr), 1,3-bis(dialkylamino)-5-methylene-1,3-diboracyclohexanes 8a, b, 1,3-bis(diethylamino)-5-methyl-1,3-dibora-4-cyclo-hexene (10), and 1,4-bis(dialkylamino)-6-methylene-1,4-dibora-2-cycloheptenes 11a, b. The compounds 2b, 8b, and the 2,3-biboratafulvene derivative [Li(TMEDA)]2[CH2C(CHB)2-(NiPr2)2] are characterized by X-ray diffraction analysis. It is shown that for trigonal boron B - C(allyl) bond distances (typically 160 ± 1 pm) are significantly larger than B - C(alkyl) distances (typically 158 + 1 pm).
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1589-1595 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Electron-Excess Complexes of Cobalt and Nickel with Cyclobutadiene Ligands: Syntheses, Cyclovoltammetry, and Reactivity[1]A cyclovoltammetric investigation of tetraphenylcyclobutadiene complexes [ML(C4Ph4)]+ [1: ML = NiCp; 2a: ML = Co(C6H6); 2b: ML = Co(mesitylene)] reveals a reversible reduction to paramagnetic complexes 1 and 2a,b with a 19-electron count, and a subsequent irreversible reduction to anions 1- and 2a,b- with a 20-electron shell. Preparative reduction by one equivalent of CpFe(HMB) (HMB = C6Me6) produces the novel 19-electron complexes 1 and 2b. Complex 1 can also be obtained by treatment of 1 · Br with one equivalent of CoCp2 at room temperature while reduction at -20°C with two equivalents of CoCp2 affords a novel C-C-linked adduct CpNi[μ,η3:η4-(C4Ph4-C5H5)]CoCp (5). Above -10°C a slow equilibrium between 5 and its components 1 and CoCp2 is observed with ΔH = 15 kJ/mol for the dissociation process. With an excess of the stronger reductant sodium amalgam the cations 1+ and 2a+ are reduced to give cyclobutenyl complexes ML(η3-1,2,3,endo-4-C4HPh4) [6: ML = NiCp; 7: ML = Co(C6H6)]. 1 reacts with p-nitrobenzyl bromide to give 1 Br and a p-nitrobenzyl addition product CpNi[η3-exo-4-(p-O2NC6H4CH2)-1,2,3,endo-4-C4Ph4] (11) while 2b reacts with MeI to give 2b · I and two isomeric methyl addition products (η5-1,3,5,exo-6-C6H3Me4)Co(C4Ph4)] (12) and (mes)Co(η3-exo-4-Me-1,2,3,endo-4-C4Ph4) (13). Sodium-amalgam reduction of the tetramethylcyclobutadiene cations [(arene)Co(C4Me4)]+ (4a: arene = C6H6; 4b: arene = mesitylene) affords diamagnetic dinuclear compounds of type 8-10 with C-C linkages between C4Me4/C4Me4, arene/C4Me4, and arene/arene rings, respectively.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    Location Call Number Expected Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...