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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 3619-3622 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Amino-äthylphosphine, die sowohl P—H- als auch N—H-Funktionen besitzen, reagieren mit Aldehyden und Ketonen unter cyclisierender Kondensation zu 1.3-Azaphospholidinen (1-2), deren Struktur IR-spektroskopisch sowie nach Umsetzung mit Schwefel als P-Sulfide (13) bzw. Dithiophosphinsäuren (14, 15) mit Betainstruktur bewiesen wurde.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 4032-4035 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Durch radikalische Addition von Butyl- bzw. Phenylphosphin an Allylamin werden [3-Aminopropyl]-butyl- (1) und [3-Amino-propyl]-phenyl-phosphin (2) erhalten. 1 und 2 reagieren mit Carbonylverbindungen unter cyclisierender Kondensation zu Perhydro-1.3-azaphosphorinen (4 - 9), die durch Umsetzung mit HCl zu entsprechenden Hydrochloriden und durch Oxydation mit Schwefel zu P-Sulfiden charakterisiert werden.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0044-2313
    Keywords: α-Functionalized methylphenyl phosphines ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Functionalized 2-Methylphenyl Phosphines, 2-(HE—CH2)—C6H4—PH2 (E: O, NR, PH) I. Preparation, Deprotonation and Silylation BehaviourBy reaction of different ortho-substituted phenyl phosphonates 2-X—C6H4—PO3R2 (X = COOR, CONHR, PO3R2) with LiAlH4 α-functionalized 2-methylphenyl phosphines 2-(HE—CH2)—C6H4—PH2 (E: O, NPh, PH) are accessible. The title compounds are characterized by deprotonation and silylation experiments.
    Notes: Durch Reduktion verschieden ortho-substituierter Benzolphosphonsäureester 2-X—C6H4—PO3R2 (X = COOR, CONHR, PO3R2) mit LiAlH4 werden die α-funktionellen 2-Methylphenylphosphane 2-(HE—CH2)—C6H4—PH2 (E: O, NPh, PH) zugänglich. Deren Metallierungs- und Silylierungsverhalten wird 31P-NMR-spektroskopisch untersucht.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0009-2940
    Keywords: Benzo-1,3,2-diphosphaborolanes ; Benzo-1,3,2-diphosphaborolane dimmers ; Benzo-1,4,2,3-diphosphadiborinanes ; Rearrangement reaction ; Pentacarbonyl chromium complexes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A series of benzo- 1,3,3-diphosphaborolanes C6H4(PR)2BR' (R = H, iPr, SiMe3; R' = R2N, R) has been prepared by several routes and characterized by spectroscopic and - in part - by X-ray diffraction methods. They feature pyramidal P atoms with the substituents in antiperiplanar positions. The P atoms act as coordination sites for the (CO)5Cr fragment. In contrast to the R2N-bearing benzo-1,3,2-diphosphaborolanes, the derivative C6H4(PH)2BCMe3 (4f) dimerizes by additional B-P bond formation to produce a pentacyclic system (4f)2. - The reaction of C6H4(PHNa)2 with B2(NMe2)2Cl2 in THF/hexane yields the acyclic phosphanylborane Me2NB(PH-C6H4PH2)2 (15). However, if C6H4[P(iPr)Li]2 is allowed to react with B2(NMe2)2Cl2, the benzo-1,4,2,3-diphosphadiborinane 13 is obtained, together with its rearrangement product 2-bis(dimethylamino)borylbenzo-1,3,2-diphosphaborolane 14 which dimerizes to (14)2.  -  In contrast, the almost planar ring of the 2,3-dimesitylbenzo-1,4,2,3-diphosphadiborinane (16) possesses P and B atoms with a planar geometry. Short B-B and B-P bonds suggest that this new heterocycle can be regarded as a 6π electron system. Moreover, the benzo-1,5,2,3,4-diphosphatriborepane 18 forms readily forms readily from C6H4(PHNa)2 and Br(Me2N)B-B(N-Me2)-B(NMe2) Br to give a tub-shaped seven-membered C2B3P2 ring system with the P atoms in a pyramidal and the B atoms in a planar environment.
    Additional Material: 10 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 621 (1995), S. 1605-1609 
    ISSN: 0044-2313
    Keywords: Carbonyl coordination compounds ; α-Functionalized 2-methyl phenylphosphines ; W(CO)5 shift ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: α-Functionalized 2-Methyl Phenylphosphines, 2-(HE—CH2)—C6H4—PH2 (E = O, NR, PH) II. Coordination Behaviour with Metal Carbonyles of Cr, Mo, WThe preparation of different carbonyl substituted coordination compounds (M: Cr, Mo, W) of the phosphines 2-(HE—CH2)C6H4—PH2 (E = O, NPh, PH) is described. In one case, after deprotonation of a PH2 group a phosphine/phosphide migration of a W(CO)5 fragment is detected.
    Notes: Von drei α-funktionellen Methylphenylphosphanen 2-(HE—CH2)C6H4—PH2 (E = O, NPh, PH) werden Carbonylkomplexe der Metalle Cr, Mo, W beschrieben. In einem Fall wird nach Metallierung die Wanderung eines phosphano-koordinierten W(CO)5-Fragmentes an ein bereits W(CO)5-koordiniertes Phosphid beobachtet.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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