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  • 1
    ISSN: 1434-4475
    Keywords: Copper complex ; Phosphazene ; (Aminomethyl)pyridine ; N-Donor ligand
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Reaktion von Monochlorpentaphenoxycyclotriphosphazen mit 3-(Aminomethyl)pyridin ergibt 3-(Aminomethyl)pyridylpentaphenoxycyclotriphosphazen (1), einen neuen N-Donor Liganden mit fünf Strickstoffatomen als potentielle Metallkoordinationszentren. Bei der Umsetzung von1 mit Kupfer(II)nitrat entsteht der Metallkomplex2 mit der Zusammensetzung Cu(1)2(NO3)2. Die durch Röntgenstrukturanalyse ermittelte Molekülstruktur zeigt, daß das Kupferion von zwei Stickstoffatomen der Pyridinringe sowie vier Sauerstoffatomen der unsymmetrisch zweizähnigen NitratgruppenJahn-Teller-verzerrt oktaedrisch umgeben ist.
    Notes: Summary The reaction of monochloropentaphenoxycyclotriphosphazene with 3-(aminomethyl)pyridine yields 3-(aminomethyl)pyridylpentaphenoxycyclotriphosphazene (1), a new N-donor ligand with five nitrogen atoms as potential coordination centers. Complex formation with copper(II) nitrate yields compound2 with the general structure Cu(1)2(NO3)2. The X-ray structure analysis shows that the copper ion is coordinated by two nitrogen atoms of the pyridine rings and four oxygen atoms of the unsymmetrical bidentate nitrate groups in aJahn-Teller distorted octahedral arrangement.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 51 (1995), S. 670-673 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 51 (1995), S. 1215-1218 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 913-918 
    ISSN: 0044-2313
    Keywords: Phosphazenes ; phosphorus-hydrazine ring systems ; twist-conformations ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N-Alkylated Pihydrazidophosphoric Acid Esters and Hexachlorocyclotriphosphaza-l,3,5-triene: Building Blocks of Spirocyclic SystemsIn contrast to secondary amines the N-alkylated di hydrazidophosphoric acid derivatives reported here attack hexachlorocyclotriphosphaza-l,3,5-triene exclusively at geminal positions and therefore react to spirocyclic systems. The synthesis and spectroscopic characterization of 4′,4′,6′,6′-tetrachloro-2-phenoxy-l,3,7,9-tetraaza-2λ5,8λ5-diphosphatricyclo[7.3.0.03.7]dodecane-spiro[8.2′]-cyclotri(phosphazene)-2-sulfide (Cl4N3P3(N(CH2)3N)2P(S)OC6H5) (1) and 4,4,6,6-Tetrachloro-l′,2′,4′,5′-tetramethyl-6′-phenoxycyclotri-(phosphazene)-spiro[2.3′]-cyclodi(λ5-phosphadiazane)-6′-sulfide (Cl4N3P3(NCH3NCH3)2P(S)OC6H5) (2) are described. The molecular structures of 1 and 4,4,6,6-Tetrachloro-1′5′-dimethyl-6′-phenoxycyclotri(phosphazene)-spiro[2.3′]-cyclodi(λ5-phosphadiazan)-6′-sulfide (Cl4N3P3(NHNCH3)2P(S)OC6U5) (3) were determined by X-ray single crystal structure analysis and show that the six-membered phosphorus-hydrazine rings of both compounds adopt twist-conformations.
    Notes: Im Gegensatz zu sekundären Aminen greifen die beschriebenen N-alkylierten Dihydrazidoderivate der Phosphorsäure Hexachlorcyclotriphosphaza-l,3,5-trien ausschließlich geminal an und reagieren daher zu spirocyclischen Systemen. Die Synthese und spektroskopische Charakterisierung von 4′,4′,6′,6′-Tetrachloro-2-phenoxy-l,3,7,9-tetraaza-2λ5,8λ5-diphosphatricyclo[7.3.0.03.7]dodecanspiro[8.2′]cyclotri(phosphazen)-2-sulfid (Cl4N3P3(N(CH2)3N)2P(S)OC6H5) (1) und 4,4,6,6-Tetrachloro-1,2′,4′,5′-tetramethyl-6′-phenoxycyclotri(phosphazen)-spiro[2.3′]-cyclodi(λ5-phosphadiazan)-6′-sulfid (Cl4N3P3(NCH3NCH3)2P(S)OC6H5) (2) werden beschrieben. Die Molekülstrukturen von 1 und von 4,4,6,6-Tetrachloro-l′5′-dimethyl-6′-phenoxycyclotri(phosphazen)-spiro[2.3′]-cyclodi(λ5-phosphadiazan)-6′-sulfid (Cl4N3P3(NHNCH3)2P(S)OC6H5) (3) wurden durch Röntgenstrukturanalysen an Einkristallen ermittelt und ergeben, daß die Phosphor-Hydrazin-Baueinheiten beider Verbindungen in Twistkonformationen vorliegen.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 1434-1438 
    ISSN: 0044-2313
    Keywords: Spiro compounds ; phosphazenes ; phosphorus hydrazine heterocycles ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Substitution Products of 4,4,6,6-Tetrachloro-6′-phenoxy-6′ -thioxo-cyclotriphosphazene-2-spiro-3′-cyclodi(phosphadiazane)Reactions of the spiro compound 4,4,6,6-Tetrachloro-6′-phenoxy-6′-thioxo-cyclotriphosphazene-2-spiro-3′-cyclodi(phosphadiazene) Cl4N3P3(NH—NH)2P(S)OC6 H5 with an excess of ammonia, cyclopropylamine, aziridine, and sodium phenolate were investigated. Fully or partially substitution of the chlorine atoms occurs. The reaction with two equivalents of the aziridine yields a mixture of isomers which consists of two geminal and two vicinal disubstituted products.The constitutions of the substituted compounds were confirmed by IR, NMR, MS and elemental analyses.
    Notes: Reaktionen der Spiroverbindung 4,4,6,6-Tetrachlor-6′-phenoxy-6′ -thioxo-cyclotriphosphazen-2-spiro-3′-cyclodi(phosphadiazan) Cl4N3P3(NH—NH)2P(S)OC6 H5 mit Ammoniak, Cyclopropylamin, Aziridin und Natriumphenolat werden untersucht. Sie führen zu teilweiser oder vollständiger Substitution der Chloratome am Phosphazenring. Die Umsetzung mit zwei äquivalenten Aziridin ergibt ein Isomerengemisch, das aus zwei geminal und zwei vicinal disubstituierten Produkten besteht.Die Konstitutionen der Substitutionsprodukte werden durch IR-, NMR- und Massenspektren sowie durch Elementaranalysen belegt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 609 (1992), S. 67-70 
    ISSN: 0044-2313
    Keywords: 4,4,6,6,-Tetrachloro-1′ ; 5′-dimethyl-6′-phenoxy-6′-thioxo-cyclotriphosphazene-2-spiro-3-cyclodi-[phosphadiazane] ; 4,4,6,6,8,8-hexachloro-6′-phenoxy-6′-thioxo-cyclotetraphosphazene-2-spiro-3′-cyclodi[phosphadiazane] ; spiro-phosphazanes; phosphorus-hydrazine heterocycles ; 31P-NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: New Spiro Compounds from Cyclophosphazenes and Cyclodi[phosphadiazanes]Chlorocyclophosphazenes (Cl2P = N)3 and (Cl2p = N)4 react with dihydrazidophosphoric acid derivatives in THF in the presence of triethylamine to give the spirocyclic compounds Cl4N3P3(NHN(CH3))2P(S)OC6H5, Cl6N4P4(NHNH)2P(S)OC6H5. Constitutions have been confirmed by MS, NMR, IR and elemental analysis.
    Notes: Chlorocyclophosphazene (Cl2P=N)3 und (Cl2p = N)4 reagieren mit Dihydraazidophosphorsäure-derivaten in THF in Gegenwart von Triethylamin zu den Spiroverbindungen Cl4N3P3(NHN(CH3))2P(S)OC6H5, Ci6N4P4(NHNH)2P(s) OC6H5. Die Konstitutionen der neuen Verbindungen wurden durch IR-, NMR- und Massenspektren sowie durch Elementaranalysen belegt.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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