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  • 1
    ISSN: 0044-2313
    Keywords: 1,4,2λ5,5λ5-Dioxadiphosphorinane ; NMR-Spectra ; Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: P,P′-(2,5-Dimethoxy-3,6-dimethyl-2,5-dioxo-2λ5,5λ5-[1,4,2,5]dioxadiphosphinane-2,5-diyl)-bis-phosphonic acid tetramethylesterThe title compound 1 is formed by reaction of the corresponding phosphonic acid 2 and orthoformicacidmethylester as a mixture of four stereoisomeres. The RRSS isomer was separated. It crystallizes in the triclinic space group P -1 with a = 649.2 pm, b = 976.1 pm, c = 1 571.7 pm, α = 80.9°, β = 88.1°, γ = 78.6° and Z = 2. The 31P and 13C NMR spectra (4 and 5 spin systems) are discussed.
    Notes: Die Titelverbindung 1 entsteht aus der zugrundeliegenden Phosphonsäure 2 und Orthoameisensäuremethylester als Gemisch aus vier Stereoisomeren, von denen das RRSS-Isomer präparativ abgetrennt werden konnte. Dieses kristallisiert triklin in der Raumgruppe P -1 mit a = 649,2 pm, b = 976,1 pm, c = 1 571,7 pm, α = 80,9°, β = 88,1°, γ = 78,6° und Z = 2. Die 4- und 5-Spinsysteme der 31P- und 13CNMR-Spektren werden analysiert.
    Additional Material: 2 Ill.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1038-1046 
    ISSN: 0044-2313
    Keywords: Binuclear antimony(V) complexes ; structure ; dynamics ; NMR spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: d, h-μ-Benzylalkoxophosphonato-e-μ-alkoxo-f-μ-oxo-bis[trichloroantimony(V)] CompoundsThe binuclear antimony(V) complexes Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 - 6 with R1 = R2 = CH3, C2H5 and R3 = C6H5CH2, (CH3)3C6H2CH2 in solution slowly exchanges the R2 groups between the oxygen atoms of the Sb2O2 ring. The SbOPOSb ringsystem makes rapid pseudorotation. The isomeres are detected by nmr spectroscopy. 1 (R1 = R2 = CH3) crystallizes in the orthorhombic space group Pnma with a = 1247.0, b = 1324.1, c = 1207.9 pm and Z = 4. 2 (R1 = CH3, R2 = C2H5) and 5 (R1 = R2 = CH3, R3 = (CH3)3 · C6H2CH2) crystallizes triclinic in the space group P-1 with a = 984.1, b = 1026.7, c = 1079.9 pm, α = 87.93, β = 75.70, γ = 87.62° and Z = 2 and a = 1164.6, b = 1296.9, c = 1712.9 pm, α = 109.9, β = 96.3, γ = 100.2° and Z = 4 resp., with two crystallographically independent molecules in the asymmetric unit.
    Notes: Die zweikernigen Antimon(V)-Komplexe Cl3Sb(O)[R3(R1O)PO2](OR2)SbCl3 1 bis 6 mit R1 = R2 = CH3, C2H5 und R3 = C6H5CH2, (CH3)3C6H2CH2 tauschen bei RT in Lösung langsam die R2-Gruppen aus. Daneben erfolgt rasches Umklappen des SbOPOSb-quasi-Fünfringes. Die Isomerenbildung wird NMR-spektroskopisch nachgewiesen. 1 (R1 = R2 = CH3) kristallisiert orthorhombisch in der Raumgruppe Pnma mit a = 1247,0, b = 1324,1, c = 1207,9 pm und Z = 4. 2 (R1 = CH3, R2 = C2H5) und 5 (R1 = R2 = CH3, R3 = (CH3)3C6H2CH2) kristallisieren triklin in der Raumgruppe P-1 mit a = 984,1, b = 1026,7, c = 1079,9 pm, α = 87,93, β = 75,70, γ = 87,62° und Z = 2 bzw. a = 1164,6, b = 1296,9, c = 1712,9 pm, α = 109,9, β = 96,3, γ = 100,2° und Z = 4 mit zwei kristallographisch unabhängigen Molekülen in der asymmetrischen Einheit.
    Additional Material: 4 Ill.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 623 (1997), S. 1633-1638 
    ISSN: 0044-2313
    Keywords: (CH3)2S derivatives ; Structure ; Spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: (CH3)2SBr2 - Reactions and Structures(CH3)2SBr2 (1) is a donor acceptor complex (8-S-3 + 10-Br-2) which reacts with (CH3)2S(=O)NSi(CH3)3 to yield [(CH3)2S(O)=N—S(CH3)2]+Br- (2). With SbBr3 (CH3)2SBr+SbBr4- (3) can be isolated. 1 crystallizes monoclinic in the space group P21/c with a = 733.8, b = 734.2, c = 1132.7 pm, β = 92.8° and Z = 4. 2 crystallizes in the orthorhombic space group Pnma with a = 967.2, b = 793.3, c = 1168.3 pm and Z = 4. The SBr and BrBr force constants of 1 are compared with those of S2Br2, 3 and Br2 resp. The nmr and mass spectra of 1 and 2 are communicated.
    Notes: (CH3)2SBr2 (1) ist ein (8-S-3 + 10-Br-2) Donor-Akzeptor-Komplex(8-S-3 + 10-Br-2) bedeutet: acht Valenzelektronen am S-Atom, das von drei Bindungspartnern umgeben ist, und zehn Valenzelektronen am Br-Atom, das zwei Bindungspartner hat; s.: S. W. Perkins, J. C. Martin, A. J. Arduengeo III, W. Lau, A. Alegria, J. K. Kochi, J. Am. Chem. Soc. 1980, 102, 7753. und reagiert mit (CH3)2S(=O)NSi(CH3)3 zu [(CH3)2S(O)=N—S(CH3)2]+Br- (2), mit SbBr3 zu (CH3)2SBr+SbBr4- (3). 1 kristallisiert monoklin (P21/c) mit a = 733,8, b = 734,2, c = 1132,7 pm, β = 92,8° und Z = 4. 2 kristallisiert orthorhombisch in der Raumgruppe Pnma mit a = 967,2, b = 793,3, c = 1168,3 pm und Z = 4. Die SBr- und BrBr-Kraftkonstanten von 1 werden mit denen von S2Br2 und 3 bzw. Br2 verglichen. Die NMR- und Massenspektren von 1 und 2 werden kurz diskutiert.
    Additional Material: 2 Ill.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 409 (1974), S. 129-136 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Spectroscopic Studies of Antimony(V) EthoxidesThe 1H-NMR and the vibrational spectra of Na(Sb(OC2H5)6), (Sb(OC2H5)5)2, Sb(OC2H5)5 · NH3, (SbCl4OC25)2 and SbCl5 · C2H5OH were measured and discussed in view of structure and bonding.
    Notes: Die 1H-NMR- und die Schwingungsspektren des Natrium-hexaäthoxiantimonats(V), des dimeren Antimonsäurepentaäthylesters, dessen 1:1-Adduktes mit Ammoniak, des dimeren Antimontetrachloridäthoxids sowie des 1:1-Adduktes aus Antimon(V)-chlorid und Äthanol wurden aufgenommen und im Hinblick auf Struktur und Bindungsverhältnisse diskutiert.
    Additional Material: 2 Ill.
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 422 (1976), S. 266-272 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction Products of Chloromethoxiphosphines and Antimony (V) Chloride. Vibrational Spectra of the 1:1-adducts of Methoxiphosphoryl Compounds and Antimony (V) ChlorideChloromethoxiphosphines react with antimony(V) chloride in a redox process to yield the chloromethoxiphospllonium hexachloroantimonates(V) (CH3O)3PCl2+SbCl6- (II) and CH3OPCl3+SbCl6- (III). II, III, (CH3O)3PCl+SbCl6-(1) and (CH3O)4P+SbCl6- eliminate easily methyl chloride and give the addition compounds OP(OCH3)3·SbCl5(IV), OPCl(OCH3)2 · SbCl5 (V), OPCl2(OCH3)·SbCl5 (VI) and OPCl3·SbCl5 (VII). The vibrational spectra of IV, V nnd VI are discussed.
    Notes: Chlormethoxiphosphine reagieren mit Antimon(V)-chlorid in einer Redoxreaktion zu Chlormethoxiphosphonium-hexachloroantimonaten(V) (CH3O)2PCl2+SbCl6-(II) und CH3OPCl3+SbCl6-(III). II, III, (CH3O)3PCl+SbCl6 (I) und (CH3O)4P+SbCl6 spalten leicht Methylchlorid ab und gehen in die 1:1-Additionsverbindungen OP(OCH3)3 · SbCl5 (IV), OPCl(OCH3)2 · SbCl5 (V), OPCl2(OCH3) · SbCl5 (VI) und OPCl3 · SbCl5 (VII) über. Die Schwingungsspektren von IV, V und VI werden diskutiert.
    Additional Material: 1 Ill.
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 428 (1977), S. 209-221 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Chloroantimony(V) PhosphatesThe 1:1 adducts of alkoxiphosphoryl compounds and antimony(V) chloride eliminate alkylchloride to yield the dimere tetrachloroantimony(V) phosphates [Cl4SbO2PCl2]2 I, [Cl4SbO2P(OCH3)Cl]2 II, [Cl4SbO2P(OCH3)2]2 III, [Cl4SbO2P(OC2H5)Cl]2 IV, [Cl4SbO2P(OC2H5)2]2 V and the tetramere trichloroantimony(V) phosphates [Cl3SbO3POCH3]4 VI resp. [Cl3SbO3POC2H5]4 VII. III can also be prepared by reaction of K+O2P(OCH3)2- with SbCl5. The vibrational spectra, the 1H- and the 31P-n.m.r. data of II, IV, V, VI and VII are communicated.
    Notes: Durch Alkylchloridelimineriung aus 1:1-Addukten aus Alkoxyphosphorylverbindungen und Antimon(V)-chlorid lassen sich die dimeren Tetrachloroantimon(V)-phosphate [Cl4SbO2PCl2]2 I, [Cl4SbO2P(OCH3)Cl]2 II, [Cl4SbO2P(OCH3)2]2 III, [Cl4SbO2P(OC2H5)Cl]2, IV, [Cl4SbO2P(OC2H5)]2 V sowie die tetrameren Trichloroantimon(V)-phosphate [Cl3SbO3POCH3]4 VI und [Cl3SbO3POC2H5]4 VII darstellen. III wurde auch durch Umsetzung von K+O2P(OCH3)2- mit SbCl5 erhalten. Die Schwingungsspektren von II, IV, V, VI und VII sowie die 1H- und die 31P-NMR-Daten werden mitgeteilt.
    Additional Material: 3 Ill.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 441 (1978), S. 213-215 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Azidomethoxi Bis(dimethylamino)phosphonium Hexachloroantimonate(V)Azidomethoxibis(dimethylamino)phosphonium hexachloroantimonate(V) I is prepared by reaction of azidobis(dimethylamino)phosphate and trimethyloxonium hexachloroantimonate(V). It decomposes thermally to the 1:1 addition compound of azidobis(dimethylamino)-phosphate and antimony(V) chloride II. The i. r. spectra and the chemical shift of phosphorus of I and II are communicated.
    Notes: Azidomethoxibis(dimethylamino)phosphonium-hexachloroantimonat(V) I wird durch Methylierung des Azidobis(dimethylamino)phosphats mit Trimethyloxonium-hexa-chloroantimonat(V) erhalten. I zerfällt thermisch in das 1:1-Addukt aus Azidobis(dimethylamino)-phosphat und Antimon(V)-chlorid II. Das IR-Spektrum und die chemische Verschiebung des Phosphorsignals von I und II werden mitgeteilt.
    Additional Material: 1 Tab.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 467 (1980), S. 197-202 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Reaction of Antimony(V) Chloride with Sulphonic and Sulphuric Acid Methylester, resp.Reaction of antimony(V) chloride with methyl and trifluoromethyl sulphonic acid methylester, resp., yields by methylchloride elimination the dimeric tetrachloroantimony(V) methane sulphonates Dimethyl sulphate reacts in dependence of the molar ratio of the components to the dimeric tetrachloroantimony(V) methyl sulphate and the polymeric bis(tetrachloroantimony(V)) sulphate, resp. The vibrational spectra are discussed.
    Notes: Antimon(V)-chlorid bildet mit Methan- bzw. Trifluormethansulfonsäure-methylester unter Methylchlorideliminierung die dimeren Tetrachloroantimon(V)-methansulfoante Mit Dimethylsulfat entsteht in Abhängigkeit vom Molverhältnis der Reaktanden das ebenfalls dimere Tetrachloroantimon(V)-methylsulfat bzw. das polymere Bis(tetrachloroantimon(V))-sulfat. Die Schwingungsspektren werden angegeben und diskutiert.
    Additional Material: 2 Tab.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 514 (1984), S. 137-148 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Dialkylaminostibanes. Preparation and SpectraThe dialkylaminodichlorostibanes Cl2SbNMe2 (1), Cl2SbNMeEt (2), and Cl2SbNEt2 (3) as well as the bis(dialkylamino) chlorostibanes ClSb[NMe2]2 (4), ClSb[NMeEt]2 (5), and ClSb[NEt2]2 (6) were prepared by exchange reactions between SbCl3 and Sb[NRR′]3 (R = R′ = Me (7); R = R′ = Et (8); R = Me, R′ = Et (9). By reaction of 1 and 2 with MeOH and EtOH the dialkylaminoalkoxochlorostibanes ClSbOMe[NMe2] (10), ClSbOEt[NMe2] (11), and ClSbOEt[NMeEt] (12) can be prepared. The vibrational spectra of 1-12 were assigned and discussed. 1-4 and 10-12 were associated in the solid state by SbN-bridges to dimeres. An analog association is sterically hinderd for 5-9.
    Notes: Durch Austauschreaktionen werden aus Antimon(III)-chlorid und den Trisdialkylaminostibanen Sb[NMe2]3 (7), Sb[NEt2]3 (8) und Sb[NMeEt]3 (9) die bisher unbekannten Dialkylaminochlorostibane Cl2SbNMe2 (1), Cl2SbNMeEt (2) und Cl2SbNEt2 (3) sowie die Bis(dialkylamino) chlorostibane ClSb[NMe2]2 (4), ClSb[NMeEt]2 (5) und ClSb[NEt2]2 (6) dargestellt. 1 und 2 ergeben mit MeOH bzw. EtOH die Dialkylaminoalkoxochlorostibane ClSbOMe[NMe2] (10), ClSbOEt[NMe2] (11) und ClSbOEt[NMeEt] (12). Die Schwingungsspektren von 1-12 werden zugeordnet und diskutiert. Danach sind 1-4 und 10-12 über SbN-Brückenbindungen im Feststoff zu Dimeren assoziiert. 5-9 sind monomer, Brückenbindungen sind aus sterischen Gründen nicht möglich.
    Additional Material: 6 Tab.
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  • 10
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N, N′ substituted Dimethylbenzamidines C6H5C(NCH3)2ElCl4(El = P, As, Sb). Structures and SpectraThe crystal and molecular structure of C6H5C(NCH3)2ElCl4 (El = P (1), As (2), Sb (3)) are determined by X-ray method. The fine differences in the structures are analysed. The 1H, 31P, and 13C NMR data are communicated. 1, 2, and 3 are examined by mass spectrometry. The different intensities of the fragments are discussed and fragmentation mechanisms are proposed.
    Notes: Die Kristall- und Molekülstruktur von C6H5C(CNH3)2ElCl4 (El = P (1), As (2), Sb (3)) wird röntgenstrukturanalytisch ermittelt. Die Struktureigenheiten werden diskutiert. Die 1H-, 31P- und 13C-Kernresonanzdaten werden mitgeteilt. Von 1 - 3 wurden Massenspektren angefertigt. Die unterschiedliche Häufigkeit der Bruchstücke wird diskutiert und für einige Ionen werden Bildungswege vorgeschlagen.
    Additional Material: 2 Ill.
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