Library

X
You have 0 saved results.
Mark results and click the "Add To Watchlist" link in order to add them to this list.
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
    Darstellung und Reaktionen von Natriumtellurid, Na2Te - Kristallstruktur von [Na(CH3OH)3]2Te2Professor Gerhard Thiele zum 60. Geburtstag gewidmet (1996)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 231-234 
    Details
    ISSN: 0044-2313
    Keywords: Sodium tellurides ; dialkyl tellurides ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Reactions of Sodium Telluride, Na2Te - Crystal Structure of [Na(CH3OH)3]2Te2Sodium telluride, Na2Te 1, is easily obtained by reaction of sodium with hexagonal tellurium in 1,2-dimethoxy-ethane in the presence of catalytic amounts of naphthalene. Upon exposure to oxygen 1 reacts with methanol forming [Na(CH3OH)3]2Te2 2, which crystal structure was determined. Compound 1, prepared in situ, can be conveniently converted into dialkyl tellurides, R2Te (R = C2H5, i-C3H7, CH2 = CH—CH2 3).
    Notes: Natriumtellurid, Na2Te 1, läßt sich auf bequeme Art und Weise aus Natrium und hexagonalem Tellur in 1,2-Dimethoxy-ethan als Reaktionsmedium in Anwesenheit katalytischer Mengen an Naphthalin gewinnen. Bei der Einwirkung von Sauerstoff auf 1 in Gegenwart von Methanol entsteht [Na(CH3OH)3]2Te2 2, dessen Kristallstruktur ermittelt wurde. In situ gewonnenes 1 kann auf einfache Weise in Dialkyltelluride, R2Te, übergeführt werden (R = C2H5, i-C3H7, CH2 = CH—CH2 3).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19966220205
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    Synthese und Kristallstruktur des Tellur-Nitridchlorids [Te11N6Cl26]Frau Professor Marianne Baudler zum 75. Geburtstag gewidmet (1996)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 739-744 
    Details
    ISSN: 0044-2313
    Keywords: Tellurium ; Nitride Chloride ; Synthesis ; IR spectra ; Crystal Structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Crystal Structure of the Tellurium Nitride Chloride [Te11N6Cl26]The title compound has been prepared by the reaction of tellurium tetrachloride with tris(trimethylsilyl)amine in boiling toluene. Pale yellow crystals of the composition [Te11N6Cl26]2 · 9C7H8 are obtained by cooling of the saturated solution. The compound was characterized by IR spectroscopy and by a crystal structure determination. Space group P1, Z = 1, structure solution with 5912 observed unique reflections, R = 0.043. Lattice dimensions at -50°C: a = 1636.2, b = 1692.7, c = 1704.1 pm, α = 60.57°, β = 69.59°, γ = 64.29°. The dominating structural element of the nitrchloride are planar Te5N3 units forming two four-member Te2N2 rings which are condensed together. Two asymmetric units [Te11N6Cl26] are linked by a centre of symmetry; the intercalated toluene molecules are without binding interactions.
    Notes: Die Titelverbindung entsteht durch Reaktion von Tellurtetrachlorid mit Tris(trimethylsilyl)amin in siedendem Toluol. Blaßgelbe Kristalle der Zusammensetzung [Te11N6Cl26]2 · 9C7H8 entstehen beim Abkühlen gesättigter Lösungen. Die Verbindung wird durch das IR-Spektrum und durch eine Kristallstrukturanalyse charakterisiert. Raumgruppe P1, Z = 1, Strukturlösung mit 5912 beobachteten unabhängigen Reflexen, R = 0,043. Gitterkonstanten bei -50°C: a = 1636,2; b = 1692,7; c = 1704,1 pm; α = 60,57 β = 69,59°; γ = 64,29°. Bestimmendes Strukturmotiv des Nitridchlorids sind planare Te5N3-Einheiten, die zwei miteinander kondensierte Te2N2-Viererringe bilden. Zwei asymmetrische Einheiten [Te11N6Cl26] sind über ein Symmetriezentrum miteiander verknüpft; die eingelagerten Toluomoleküle sind ohne bindende Wechselwirkung.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19966220430
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    Die Kristallstrukturen von SeCl3 +SbCl6-, SeBr3+GaBr4-, PCl4+SeCl5- und (PPh4+)2SeCl42- · 2 CH3CN (1996)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 622 (1996), S. 1847-1853 
    Details
    ISSN: 0044-2313
    Keywords: Selenium Halides ; Crystal Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Crystal Structures of SeCl3+SbCl6-, SeBr3+GaBr4-, PCl4+SeCl5-, and (PPh4+)2SeCl42- · 2 CH3CNThe crystal structures of the title compounds were determined by X-ray diffraction.SeCl3+SbCl6-: Space group P21/m, Z = 4, structure determination with 1795 observed unique reflections, R = 0.022. Lattice dimensions at -80°C: a = 940.9, b = 1066.3, c = 1234.9 pm, β = 102.79°. The compound forms ion pairs with the structure of a double octahedron with linked surfaces. SeBr3+GaBr4-: Space group Pc, Z = 2, structure determination with 1461 observed unique reflections, R = 0.058. Lattice dimensions at -60°C: a = 660.1, b = 655.3, c = 1431.3 pm, β = 101.177°. The compound crystallizes in the SCl3[AlCl4] lattice type. Between the ions there are two relatively short Se … Br—Ga contacts.PCl4+SeCl5-: Space group Ima2, Z = 8, structure determination with 1757 observed unique reflections, R = 0.029. Lattice dimensions at -50°C: a = 1651.6, b = 1201.2, c = 1166.4 pm. The SeCl5- ions are associated to chains via interionic Se—Cl … Se contacts along the crystallographic c-axis.(PPh4+)2SeCl42- · 2CH3CN: Space group P21/n, Z = 2, structure determination with 2578 observed unique reflections, R = 0.050. Lattice dimensions at -80°C: a = 1288.5, b = 726.0, c = 2585.8 pm, β = 101.65°. The compound includes planar-tetragonal SeCl42- ions, which almost meet D4h symmetry.
    Notes: Die Kristallstrukturen der Titelverbindungen wurden röntgenographisch ermittelt.SeCl3+SbCl6-: Raumgruppe P21/m, Z = 4, Strukturlösung mit 1795 beobachteten unabhängigen Reflexen, R = 0,022. Gitterkonstanten bei -80°C: a = 940,9; b = 1066,3; c = 1234,9 pm; β = 102,79°. Die Verbindung bildet Ionenpaare mit der Struktur eines flächenverknüpften Doppeloktaeders.SeBr3+GaBr4-: Raumgruppe Pc, Z = 2, Strukturlösung mit 1461 beobachteten unabhängigen Reflexen, R = 0,058, Gitterkonstanten bei -60°C: a = 660,1; b = 655,3; c = 1431,3 pm; α = 101,17°. Die Verbindung kristallisiert im SCl3[AlCl4]-Strukturtyp. Zwischen den Ionen bestehen zwei relativ kurze Se … Br—Ga-Kontakte.PCl4+SeCl5-: Raumgruppe Ima2, Z = 8, Strukturlösung mit 1757 beobachteten unabhängigen Reflexen, R = 0,029. Gitterkonstanten bei -50°C; a = 1651,6; b = 1201,2; c = 1166,4 pm. Die SeCl5- -Ionen sind über interionische Se—Cl … Se-Kontakte entlang der kristallographischen c-Achse zu Ketten assoziiert.(PPh4+)2SeCl42- · 2CH3CN: Raumgruppe P21/n, Z = 2, Strukturlösung mit 2578 beobachteten unabhängigen Reflexen, R = 0,050. Gitterkonstanten bei -80°C: a = 1288,5; b = 726,0; c = 2585,8 pm; β = 101,65°. Die Verbindung enthält planar-quadratische SeCl42--Ionen, die nahezu D4h-Symmetrie erfüllen.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19966221108
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 4
    Electronic Resource
    Electronic Resource
    Synthese und NMR-Spektren von λ5-Diphospheten Die Struktur des 2,4-Diphenyl-1,1,3,3-tetrakis(diethylamino)-1λ5,3λ5-diphosphetsProfessor Lothar Kolditz zum 60. Geburtstage gewidmet (1989)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 576 (1989), S. 81-98 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and NMR Spectra of λ5-Diphosphets. Structure of 2,4-Diphenyl-1,1,3,3-tetrakis (diethylamino)-1λ5, 3λ5-diphosphetePreparation, properties, and n.m.r. spectra of C2H5PF2[N(C2H5)2]2, CH2=PF[N(C2H5)2]2, and the diphosphetes {RC=P[N(C2H5)2]2}2 (R) = H (5a), CH3 [(5b)] are described. The λ5-diphosphete {HC=P(NR2)2}2 (R = CH3) reacts with BF3 · O(C2H5)2 to give which is transformed into by n-C4H9Li. The crystal and molecular structure of 2,4-diphenyl-1,3,3-tetrakis(diethylamino)-1λ5,3λ5-diphosphete 2 are reported and discussed.
    Notes: Darstellung, Eigenschaften und NMR-Spektren von C2H5PF2[N(C2H5)2]2, CH2=PF[N(C2H5)2]2 und der Diphosphete {RC=P[N(C2H5)2]2}2 (R = H )(5a), CH3 [(5b)] werden beschrieben. Das λ5-Diphosphet {HC=P(NR2)2}2 (R = CH3) reagiert mit BF3 · O(C2H5)2 zu das mit n-C4H9Li in übergeht. Die Kristall- und Molekülstruktur von 2,4-Diphenyl-1,1,3,3-tetrakis(diethylamino)-1λ5,3λ5-diphosphet 2 werden mitgeteilt und diskutiert.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19895760111
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 5
    Electronic Resource
    Electronic Resource
    Bemerkungen zur Synthese von Difluorphosphoranen n-Butyl-bis(dimethylamino)alkylidenphosphorane. Der Komplex {(CO)4FeC[OSi(CH3)3]CH=P(n-C4H9)[N(CH3)2]2} (1990)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 588 (1990), S. 147-166 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Remarks to the Synthesis of Difluorophosphoranes. n-Butyl-bis(dimethylamino)alkyliden-phosphoranes. Complex {(CO)4FeC[OSi(CH3)3]CH=P(n—C4H9) [N(CH3)2]2}Diethylamino-diethylaminosulfanyl-difluoro-i-butyl-phosphorane 3 is formed in the synthesis of bis(diethylamino)-difluoro-i-butyl-phosphorane from the corresponding phosphane by fluorination with SF4 as a by-product. Synthesis, NMR spectra, and reactions of n-butyl-bis(dimethylamino)alkylidene phosphoranes are reported. n-Butyl-bis(dimethylamino)-trimethylsilylmethylidenphosphorane, 17, reacts with Fe(CO)5 to give the tetracarbonyliron complex 19. The result of the X-ray structural analysis of 19 is reported and discussed.
    Notes: Diethylamino-diethylaminosulfanyl-difluor-i-butyl-phosphoran 3 entsteht als Nebenprodukt bei der Synthese von Bis(diethylamino)-difluor-i-butyl-phosphoran aus dem entsprechenden Phosphan durch Fluorierung mit SF4. Synthese, NMR-Spektren und Reaktionen von n-Butyl(bisdimethylamino)alkylidenphosphoranen werden berichtet. n-Butyl-bis(dimethylamino)-trimethylsilylmethylidenphosphoran, 17, reagiert mit Fe(CO)5 zu dem Tetracarbonyleisen-Komplex 19. Das Ergebnis der Röntgenstrukturanalyse von 19 wird mitgeteilt und diskutiert.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19905880119
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 6
    Electronic Resource
    Electronic Resource
    [Na(12-Krone-4)2]2[Ni(Se4)2] · DMF; Synthese, Kristallstruktur und magnetisches Verhalten (1992)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 615 (1992), S. 131-136 
    Details
    ISSN: 0044-2313
    Keywords: Octaselenido niccelate complex ; synthesis ; X-ray structure ; FIR spectrum ; magnetic behaviour ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: [Na(12-Crown-4)2]2[Ni(Se4)2] · DMF; Synthesis, Crystal Structure, and Magnetic BehaviourThe title compound has been prepared from NiCl2 and sodium polyselenide in dimethylformamide solution in the presence of 12-crown-4, forming black crystal needles. They were characterized by an X-ray structure determination, by FIR spectroscopy as well as by the magnetic behaviour.[Na(12-crown-4)2]2[Ni(Se4)2] · DMF crystallizes monoclinically in the space group P21, 3650 observed unique reflections, R = 0.046. Lattice dimensions at -80°C: a = 1020.3(2); b = 1889.5(2); c = 1498.7(3) pm; β = 108.29(1)°. The compound has an ionic structure, in which the sodium atoms of the [Na(12-crown-4)2]+ cations are coordinated by the oxygen atoms of the crown ether molecules in an antiprismatic fashion. The nickel atom of the anion [Ni(Se4)2]2- is surrounded by four selenium atoms of the tetraselenide chelates in an almost planar environment. The DMF molecules are inserted in the lattice without a bonding interaction. The magnetic susceptibility observed in the temperature interval 4.2 to 330K can be interpreted by means of a 3E ground term and D2 as local symmetry, which was established by X-ray crystallography.
    Notes: Die Titelverbindung wurde aus wasserfreiem Nickel(II)-chlorid und Natriumpolyselenid in Dimethylformamid in Gegenwart von 12-Krone-4 in Form schwarzer Kristallnadeln hergestellt und durch eine röntgenographische Strukturanalyse, durch das FIR-Spektrum und durch sein magnetisches Verhalten charakterisiert.[Na(12-Krone-4)2]2[Ni(Se4)2] · DMF kristallisiert monoklin in der Raumgruppe P21, 3650 beobachtete unabhängige Reflexe, R = 4,6%. Die Gitterkonstanten sind bei -80°C: a = 1020,3(2); b = 1889,5(2); c = 1498,7(3) pm; β = 108,29(1)°. Die Verbindung hat ionischen Aufbau. In den Kationen [Na(12-Krone-4)2]+ sind die Natriumatome durch die acht Sauerstoffatome der beiden Kronenethermoleküle antiprismatisch umgeben. In dem Anion [Ni(Se4)2]2- ist das Nickelatom nur annähernd planar von den vier Selenatomen der beiden Tetraselenidchelate koordiniert. Die DMF-Moleküle sind in das Gitter ohne bindende Wechselwirkung eingelagert.Die im Temperaturbereich von 4,2 bis 330 K beobachtete Abhängigkeit der magnetischen Suszeptibilität läßt sich unter der Annahme eines 3E-Grundterms und der röntgenographisch ermittelten lokalen Symmetrie D2 am Nickelatom verstehen.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19926150927
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 7
    Electronic Resource
    Electronic Resource
    Synthese, Eigenschaften und Kristallstrukturen von Magnesium-Diazadien-Komplexen (1994)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 620 (1994), S. 691-696 
    Details
    ISSN: 0044-2313
    Keywords: Magnesium complexes ; diazadiene ligands ; radical anions ; endiamides ; X-ray structure ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Properties and Crystal Structures of Magnesium Diazadiene ComplexesReactions of phenyl-substituted 1,4-diaza-1,3-butadienes (DAD) RN=CPh—CPh=NR (R = C6H5) 1a, C6H4-4-CH3 1b, C6H4-4-OCH3 (1c) with magnesium in dimethoxyethan lead to complexes of the type [Mg(DAD)2(DME)] 2a-c, with DAD ligands in form of radical anions. Furthermore, highly reactiv complexes of the composition [Mg(DAD)(DME)2] 3a-c could be obtained. The crystal structures of 2a, 3a and 3c were determined.
    Notes: Die Reaktion phenylsubstituierter 1,4-Diaza-1,3-butadiene (DAD) RN=CPh—CPh=NR (R = C6H5 1a, C6H4-4-CH3 1b, C6H4-4-OCH3 1c) mit Magnesium in Dimethoxyethan (DME) führt zu Verbindungen des Typs [Mg(DAD)2(DME)] 2a-c, in denen die DAD-Liganden als Radikalanionen gebunden sind. Außerdem enstehen äußerst reaktive Komplexe der Zusammensetzung [Mg(DAD)(DME)2] 3a-c. Die Kristallstrukturen von 2a, 3a und 3c wurden aufgeklärt.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19946200418
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 8
    Electronic Resource
    Electronic Resource
    Notiz über die Reaktion zwischen Phosphortrichlorid und SchwefelwasserstoffProfessor Josef Goubeau zum 85. Geburtstage am 31. März 1986 gewidmet (1986)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 534 (1986), S. 27-30 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Notice on the Reaction between Phosphorus Trichloride and Hydrogen SulfideThe reaction between phosphorus trichloride and hydrogen sulfide in the presence of a base yields P4S3 and [PS2Cl2]- besides other products. A reaction scheme is proposed.
    Notes: Die Reaktion zwischen Phosphortrichlorid und Schwefelwasserstoff in Gegenwart einer Base liefert P4S3 und [PS2Cl2]- neben anderen Produkten. Es wird ein Reaktionsweg vorgeschlagen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19865340305
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 9
    Electronic Resource
    Electronic Resource
    NMR-Untersuchungen an Methylphosphoniumchlorid (1987)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 554 (1987), S. 146-150 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N.M.R. Investigation of Methylphosphonium ChlorideThe n.m.r. spectra of [CH3PH3]Cl in aqueous hydrochloric acid as solvent and of [OP(CH3) (OCH2CH2Cl)OCH2—]2 in C6D6 und CD2Cl2 are described. 31P n.m.r. resonances with a line width at half height of 55 Hz are found for the H2O—HCl solutions of [CH3PH3]Cl in the solid state at 183 K.
    Notes: Die NMR-Spektren von [CH3PH3]Cl in wäßrigen HCl-Lösngen und von [OP(CH3) (OCH2CH2Cl)OCH2—]2 in C6D6 und CD2Cl2 werden beschrieben. Als Festkörper vorliegende (183 K) wäßrig-salzsaure Lösngen von [CH3PH3]Cl zeigten 31P-Resonanzlinien mit einer Halbwertsbreite von 55 Hz.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19875541119
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 10
    Electronic Resource
    Electronic Resource
    Fluor-substituierte und andere neue Carbodiphosphorane (1988)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 567 (1988), S. 23-38 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Fluoro Substituted and other New CarbodiphosphoranesSyntheses and properties of the carbodiphosphoranes [(CH3)2N]3P=C=P(CH3)[N(CH3) 2]2, (3), [(CH3)2N]2(F)P=C=P(F) [N(CH3)2]2, (7), and (C6H5)2(F)P=C=P(F)(C6H5) 2, (11), are discribed. The compounds 3, 7, and 11 as well as [(C2H5)2N]3P=C=P(CH3) [(C2H5)2N]2 are characterized by their 1H, 13C, 19F, and 31P n.m.r. and mass spectra. The crystal and molecular structures of 7 are reported.
    Notes: Synthese und Eigenschaften der Carbodiphosphorane [(CH3)2N]3P=C=P(CH3)[N(CH3)2]2, (3), [(CH3)2N]2(F)P=C=P(F)[N(CH3)2]2, (7), und (C6H5)2(F)P=C=P(F)(C6H5) 2, (11), werden beschrieben. Die Verbindungen 3, 7 und 11 sowie [(C2H5)2N]3P=C= P(CH3)[(C2H5)2N]2 sind durch ihre 1H-, 13C-, 19F- und 31P-NMR-Spektren sowie durch ihre Massenspektren charakterisiert. Die Kristall- und Molekülstruktur von 7 werden mitgeteilt.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19885670104
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...