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  • 1
    Electronic Resource
    Electronic Resource
    2,4-Dimethoxycarbonyl-1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphospheteDedicated to Professor Hans-Georg von Schnering on the occasion of his sixtieth birthday. (1991)
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 2 (1991), S. 593-599 
    Details
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,1,3,3 - Tetrakis(dimethylamino) - 1λ5,3λ5 - diphosphete, 1, reacts with cyanoformic acid methyl ester to form two isomers of the title compound 2. Properties, NMR, mass, and IR spectra of 2, as well as the molecular and crystal structure of the E isomer of 2, are described and discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hc.520020515
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  • 2
    Electronic Resource
    Electronic Resource
    Reactions of 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete with diphenylchlorophosphane and methyl iodide (1996)
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 7 (1996), S. 341-347 
    Details
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphete, 1, reacts with diphenylchlorophosphane to yield 1,1,3,3-tetrakis(dimethylamino)-4-diphenylphosphanyl-1,2-dihydro-3λ5-[1,3]diphosphetium chloride, 2, or, depending on the reaction conditions, the isomer compound 3. The cation of 2 is deprotonated by LiN[Si(CH3)3]2 to give the diphenylphosphanyl-substituted derivative of 1, i.e., compound 4. Methyl iodide adds to 1 to form 1,1,3,3-tetrakis(dimethylamino)-4-methyl-1,2-dihydro-3λ5-[1,3]diphosphetium iodide, 6. Deprotonation of 6 with n-butyllithium leads to the monomethyl derivative of 1, i.e., compound 7. Physical properties, NMR spectra, and mass spectra of compounds 2-4, 6, and 7 are described. The results of the X-ray structural analysis of 6 are reported and discussed. © 1996 John Wiley & Sons, Inc.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    1, 2λ5-azaphosphinines and a new 1λ5, 3λ5-. DiphosphinineDedicated to Prof. Shigeru Oae on the occasion of his seventy-fifth birthday. (1995)
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 6 (1995), S. 355-363 
    Details
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The 1,2-azaphosphinine, 9, and the 1,3-diphosphinine, 10, can be isolated from a mixture resulting from the reaction of 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete, 1, and ethyl isothiocyanate. The reaction of 1 with phenyl isothiocyanate yields the 1,2-azaphosphinine, 16. Mechanisms for the formation of the compounds 9, 10, and 16 are suggested. The properties, the NMR, mass, and IR spectra, and the molecular and crystal structures of 9 and 10 are described and discussed.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/hc.520060413
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  • 4
    Electronic Resource
    Electronic Resource
    Ein 1,3,5-Triphosphinantriium-IonWir danken dem Fonds der Chemischen Industrie für die Unterstützung der Arbeit.Professor Hans Georg von Schnering gewidmet (1997)
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 109 (1997), S. 2444-2445 
    Details
    ISSN: 0044-8249
    Keywords: Kationen ; Phosphorheterocyclen ; Ylide ; Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ange.19971092119
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  • 5
    Electronic Resource
    Electronic Resource
    Ein 1λ5, 3λ5, 5λ5-Triphosphabenzol-Derivat (1986)
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 98 (1986), S. 1018-1019 
    Details
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/ange.19860981122
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  • 6
    Electronic Resource
    Electronic Resource
    1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphet als Ligand in Koordinationsverbindungen (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 612 (1992), S. 56-62 
    Details
    ISSN: 0044-2313
    Keywords: 1λ5,3λ5-diphosphete ; addition compounds with GeCl2, SnCl2, (CO)5W(Z-cyclooctene) ; n.m.r., i.r., mass spectra ; X-ray structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: 1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphete as Ligand in Coordination Compounds1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphete, 1, reacts with GeCl2 · 1,4-dioxane, SnCl2, and (CO)5W(Z-cyclooctene) to give the complexes {HCP[N(CH3)2]2}2 · GeCl2, 3, {HCP[N(CH3)2]2}2 · SnCl2, 4, and {HCP[N(CH3)2]2}2 · W(CO)5, 5, respectively. The n.m.r., mass, and i.r. spectra of the new compounds as well as the crystal and molecular structures of 3 and 4 are reported and the bonding situation in compounds 3-5 is discussed.
    Notes: 1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphet, 1 bildet mit GeCl2 · 1,4-Dioxan, SnCl2 bzw. (CO)5W(Z-cycloocten) die komplexe {HCP[N(CH3)2]2}2 · GeCl2, 3, {HCP[N(CH3)2]2}2 · SnCl2, 4, bzw. {HCP[N(CH3)2]2}2 · W(CO)5, 5. Die NMR-, Massen- und IR-Spektren der neuen Verbindungen sowie die Kristall- und Molekülstruktur von 3 und 4 werden mitgeteilt und die Bindungsverhältnisse in den Verbindungen 3-5 diskutiert.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926120111
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  • 7
    Electronic Resource
    Electronic Resource
    Mono- und Bis(difluorphosphoranyl)ethylen, n-Hexyliden-fluorphosphoran und ein 2,4-Di-n-pentyl-1λ5,3λ5-diphosphetProfessor Viktor Gutmann zum 70. Geburtstage gewidmet (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 613 (1992), S. 31-35 
    Details
    ISSN: 0044-2313
    Keywords: Diaminophosphanylethylene ; mono- and bis(difluorophosphoranyl)-ethylene ; n-hexylidene-fluorophosphorane ; 2,4-di-n-pentyl-1λ5, 3λ5 -diphosphete; n. m. r., ir spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Mono- and Bis(difluorophosphoranyl)ethylene, n-Hexylidene-fluorophosphorane, and a 2,4-Di-n-pentyl-1λ5, 3λ5 -diphospheteBis(diethylamino)phosphanylethylene, 1, is converted by SF4 into bis(diethylamino)difluorophosphoranylethylene, 2. Analogously trans-1,2-bis(diphenylphosphanyl)ethylene, 3, is converted into trans-1,2-bis(difluorodiphenylphoranyl)ethylene, 4. 2 reacts with n-butyllithium to give n-hexylidene-bis(diethylamino)fluorophosphorane, 5. With more n-butyllithium, the main product n-hexylidene-bis(diethylamino)-n-butylphosphorane, 7, and the by-product 2,4-di-n-pentyl-1,1,3,3-tetrakis(diethylamino)-1λ5, 3λ5 -diphosphete, 8, are formed. With t-butyllithium 2 yields 3,3-dimethyl-butylidene-bis(diethylamino)fluorophosphorane, 6. All new compounds 1, 2, 4-8 are characterized by their nmr and ir spectra.
    Notes: Bis(diethylamino)phosphanylethylen, 1, wird durch SF4 in Bis(diethylamino)difluorphosphoranylethylen, 2, übergeführt. Auf analoge Weise entsteht aus trans-1,2-Bis(diphenylphosphanyl)ethylen, 4. 2 reagiert mit n-Butyllithium zu n-Hexyliden-bis(diethylamino)fluorphosphoran, 5, aus dem mit weiterem n-Butyllithium als Hauptprodukt n-Hexyliden-bis(diethylamino)-n-butylphosphoran, 7, und als Nebenprodukt 2,4-Di-n-pentyl-1,1,3,3-tetrakis(diethylamino)-1λ5, 3λ5-diphosphet, 8, entsteht. Mit t-Butyllithium bildet 2 3,3-Dimethyl-butyliden-bis(diethylamino)fluorphosphoran, 6. Alle neuen Verbindungen 1, 2, 4-8 werden durch ihre NMR- und IR-Spektren charakterisiert.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926130105
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  • 8
    Electronic Resource
    Electronic Resource
    o-1λ5,3λ5-Diphosphaphenylen-bis(diphenylphosphan) und seine chelatbildenden Eigenschaften (1994)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 483-488 
    Details
    ISSN: 0044-2313
    Keywords: o-1λ5,3λ5-Diphosphaphenylene-bis(diphenylphosphane) ; nickel(II) chloride chelate complex ; crystal structure ; NMR, Ir spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: o-1λ5,3λ5-Diphosphaphenylene-bis(diphenylphosphane) and its Chelating PropertiesBis(diphenylphosphanyl)acetylene and 1,1′,3,3′-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete react at higher temperatures to yield the title compound 5, which forms easily the chelate complex 6 with nickel(II) chloride.
    Notes: Bis(diphenylphosphanyl)acetylen und 1,1′,3,3′-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphet reagieren bei höheren Temperaturen zur Titelverbindung 5, die mit Nickel(II)-chlorid leicht den Chelatkomplex 6 bildet.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19946200314
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  • 9
    Electronic Resource
    Electronic Resource
    Reaktion von 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5-diphosphet mit monosubstituierten Acetylenen und Acetylen 1λ5, 3λ5-Diphosphabenzole. IVIII. Mitteilung siehe [4] (1990)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 588 (1990), S. 181-191 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reactions of 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5-diphosphete with Monosubstituted Acetylenes and Acetylene. 1λ5, 3λ5-Diphosphabenzenes. IVThe monosubstituted acetylenes H—C≡C—COOCH3 and H—C≡C—CF3 react with 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete 1 to give 1,1,3,3-tetrakis (dimethylamino)- 4-methoxycarboxylato-1λ5,3λ5-diphosphorine 3, and -4-trifluoromethyl-1λ5,3λ5-diphosphorine 5, respectively. In contrast, phenylacetylene and 1 form two isomers, namely 1,1,3,3- tetrakis(dimethyl-amino)-4-phenyl-1λ5,3λ5-diphosphorine 4a und -5-phenyl-1λ5,3λ5-diphosphorine 4b. The reaction between acetylene and 1 yields the 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphorine 6, unsubstituted at the carbon atoms of the ring. Various mechanisms are discussed for the formation of the compounds 3, 4a, 4b, 5 and 6. All new compounds are characterized by their n.m.r., mass, and i.r. spectra.
    Notes: Die monosubstituierten Acetylene H—C≡C—COOCH3 und HC≡C—CF3 reagieren mit 1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphet 1 zu 1, 1, 3, 3-Tetrakis(dimethylamino)- 4-methoxycarboxylato-1λ5,3λ5-diphosphorin 3 bzw. -4-trifluormethyl-1λ5,3λ5-diphosphorin 5. Im Gegensatz dazu bildet Phenylacetylen mit 1 zwei Isomere, nämlich 1,1,3,3- Tetrakis(dimethylamino)-4-phenyl-1λ5,3λ5-diphosphorin 4a und -5-phenyl-1λ5,3λ5-diphosphorin 4b. Acetylen und 1 reagieren zu dem an den Kohlenstoffatomen des Rings unsubstituierten 1,1,3,3-Tetrakis(dimethylamino)-1λ5,3λ5-diphosphorin 6. Für die Bildung der Verbindungen 3, 4a, 4b, 5 und 6 werden verschiedene Mechanismen diskutiert. Alle neuen Verbindungen sind durch ihre NMR-, Massen- und IR-Spektren charakterisiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19905880121
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  • 10
    Electronic Resource
    Electronic Resource
    Die Hydrolyse des 1, 1, 3, 3-Tetrakis(dimethylamino)-1λ5, 3λ5-diphosphetsProfessor Rolf Appel zum 70. Geburtstage am 25. Februar 1991 gewidmet (1991)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 601 (1991), S. 65-72 
    Details
    ISSN: 0044-2313
    Keywords: 1,1,3,3-tetrakis(dimethylamino)-1λ5,3λ5-diphosphete ; hydrolysis ; bis(dimethylamino)-phosphorylmethylidene-methyl-bis(dimethylamino)phosphorane ; bis(dimethylamino)phosphoryl-methyl(dimethylamino)phosphonylmethylene ; nmr, mass spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Hydrolysis of 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphospheteHydrolysis of 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphosphet (2) yields in the first step Bis(dimethylamino)phosphorylmethyliden-methyl-bis(dimethylamino)phosphorane (5). In the second step Bis(dimethylamino)phosphoryl-methyl(dimethylamino)phosphosphonylmethylen (6) is the main product of hydrolysis. In addition small amounts of methylphosphonic-bis(dimethylamide) (7) are formed. Properties, nmr and mass spectra of 5 and 6 are described, their mechanism of formation is discussed.
    Notes: Die Hydrolyse von 1,1,3,3-Tetrakis(dimethylamino)-1λ5, 3λ5 -diphosphet (2) führt in erster Stufe zu Bis(dimethylamino)phosphorylmethyliden-methyl-bis(dimethylamino)phosphorane (5). In zweiter Stufe wird vornehmlich Bis(dimethylamino)phosphoryl-methyl(dimethylamino)phosphosphonylmethylen (6) neben geringen Mengen von Methylphosphonsphonsäure-bis(dimethylamid) (7) gebildet. Eigenschaften, NMR- und Massenspektren von 5 und 6 sind beschrieben, ihr Bildungsmechanismus wird diskutiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19916010108
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