Library

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
    Springer
    Russian chemical bulletin 39 (1990), S. 2593-2595 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract A synthesis is reported for O,O-diethyl S-(o-carboran-9-yl) thiophosphite and its transformations were studied. A series of new carboranyl esters of seleno- and thioacids of pentavalent phosphorus acids were obtained.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1573-9171
    Keywords: S-(o-carboran-9-yl)diphenylthiophosphinite ; S-(o-carboran-9-yl)diphenylthiophosphinate ; S-(o-carboran-9-yl)diphenyldithiophosphinate ; S-(o-carboran-9-yl)-diphenylselenothiophosphinate ; synthesis ; structure
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract S-(o-Carboran-9-yl) diphenylthiophosphinite was obtained for the first time, and its structure and transformations were studied. A series of esters of thio- dithio-and selenothiophosphinic acids have been synthesized and complexes of tungsten and manganese were obtained containing the carboranylthiophosphinite ligand.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 37 (1988), S. 1967-1967 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 38 (1989), S. 180-183 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Conclusions New S-(carboran-1-yl)thiophosphates and S(carboran-1-yl)thiophosphonates were obtained by the reaction of derivatives of lithiumcarboranes with bis(dialkoxythiophosphoryl)disulfides or halo derivatives of pentavalent phosphorus.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 39 (1990), S. 1502-1504 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract New carboranyl selenophosphates and selenophosphonates have been prepared. A series of S-β-carboranylselenoethyl esters of pentavalent phosphorus acids has been prepared. These compounds hold interest as potentially physiologically active compounds.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 36 (1987), S. 2227-2227 
    ISSN: 1573-9171
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Russian chemical bulletin 41 (1992), S. 366-368 
    ISSN: 1573-9171
    Keywords: O-ethyl S,S-bis(o-carboran-9-yl) dithiophosphite ; trithiophosphate ; dithiophosphonate ; dithiophosphate
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract O-Ethyl S,S-bis(o-carboran-9-yl) dithiophosphite was prepared. The reactions of this product with sulfur, selenium, methyl iodide, and chloral were studied.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 8
    ISSN: 0044-2313
    Keywords: Phoshinophosphinidene-phosphoranes, tBu2P—P=P(Me)tBu2, tBu(Me3Si)P—P=P(Me)tBu2, tBu2P—P=P(Br)tBu2 ; Synthesis ; Structures ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Structure of Phosphinophosphinidene-phosphoranes tBu2P—P=P(Me)tBu2 1, tBu(Me3Si)P—P=P(Me)tBu2 2, and tBu2P—P=P(Br)tBu2 3A new method for the synthesis of 1 and 2 (Formulae see „Inhaltsübersicht“) is reported based on the reaction of 5 with substitution reagents (Me2SO4 or CH3Cl). The results of the X-ray structure determination of 1 and 2 are given and compared with those of 3. While in 3 one P—P distance corresponds to a double bond and the other P—P distance to a single bond (difference 12.5 pm) the differences of the P—P distances in 1 and 2 are much smaller: 5.28 pm in 1, 4.68 pm in 2. Both 1 and 2 crystallize monoclinic in the space group P21/n (Z = 4). 2 additionally contains two disordered molecules of the solvent pentane in the unit cell. Parameters of 1: a = 884.32(8) pm, b = 1 924.67(25) pm, c = 1 277.07(13) pm, β = 100.816(8)°, and of 2: a = 1 101.93(12) pm, b = 1 712.46(18) pm, c = 1 395.81(12) pm, β = 111.159(7)°, all data collected at 143 K. The skeleton of the three P atoms is bent (PPP angle 100.95° for 1, 100.29° for 2 and 105.77° for 3). Ab initio SCF calculations are used to discuss the bonding situation in the molecular skeleton of the three P atoms of 1 and 3. The results show a significant contribution of the ionic structure R2P—P(-)—P(+)(X)R2. The structure with (partially) charged P atoms is stabilized by bulky polarizable groups R (as tBu) as compared to the fully covalent structure R2P—P(X)—PR2.
    Notes: Es wird ein neuer Weg zur Bildung von tBu2P—P=P(Me)tBu2 1 und tBu(Me3Si)P—P=P(Me)tBu2 2 mitgeteilt, der auf der Umsetzung von LiP[P(tBu)2]2 5 mit Substitutionsreagenzien (Me2SO4, CH3Cl) basiert. Die Ergebnisse der Kristallstrukturuntersuchung von 1 und 2 werden mitgeteilt und mit denen des tBu2P—P=P(Br)tBu2 3 verglichen. Während in 3 der eine Abstand einer Doppelbindung entspricht und der andere einer Einfachbindung (Differenz 12,5 pm) sind die Differenzen der P—P-Abstände in 1 und 2 weit geringer, in 1 5,28 pm, in 2 4,68 pm. 1 und 2 kristallisieren beide monoklin in der Raumgruppe P21/n mit vier Formeleinheiten in der Elementarzelle. Bei 2 werden zusätzlich zwei fehlgeordnete Moleküle des Lösungsmittels Pentan in der Elementarzelle eingebaut. Parameter von 1: a = 884,32(8) pm, b = 1 924,67(25) pm, c = 1 277,07(13) pm, β = 100,816(8)°, 2: a = 1 101,93(12) pm, b = 1 712,46(18) pm, c = 1 395,81(12) pm, β = 111,159(7)°, jeweils bei der Meßtemperatur 143 K. Das Gerüst der drei P-Atome ist gewinkelt, Winkel in 1 100,95°, in 2 100,29° und in 3 auf 105,77° aufgeweitert. Mit Hilfe von ab initio SCF-Rechnungen werden die Bindungsverhältnisse im Molekülgerüst der drei P-Atome in 1 und 3 diskutiert. Es zeigt sich ein deutlicher Beitrag der ionogenen Struktur R2P—P(-)—P(+)(X)R2. Die Struktur mit separierten (Teil-)Ladungen wird durch große, polarisierte Gruppen R wie tBu im Vergleich zur (unpolaren) normalvalenten Verbindung R2P—P(X)—PR2 stabilisiert.
    Additional Material: 6 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 9
    ISSN: 0044-2313
    Keywords: Formation of Li(THF)2Et2O[Cr(CO)4{η2-(tBu2P)2P}ηt-Cr(CO)5] 2, [Cr(CO)4{η2-(tBu2P)2PH}] 3, [Cr(CO)5{η1-(tBu2P)2PH}] 4 from Cr(CO)5THF and Li(THF)2[η2-(tBu2P)2P] 1, as well as of Li(12-crown-4)2[Cr(CO)4{η2-(tBu2P)2P}] 7 from 1 and NBD · Cr(CO)4. 7 forms with Cr(CO)5THF 2, with CH3COOH 3, with EtBr [Cr(CO)4{η2-(tBu2P)2PEt}] 8, with BrCH2—CH2Br [Cr(CO)4{η2-(tBu2P)2PBr}] 9. Crystal structures of 2, 3 and 4 ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition Metal Complexes of P-rich Phosphanes and Silylphosphanes. XI. Formation, Reactions, and Structures of Chromium Carbonyl Complexes from Reactions of Li(THF)2[η2-(tBu2P)2P] with Cr(CO)5 · THF and Cr(CO)4 · NBDReactions of Li(THF)2[η2-(tBu2P)2P] 1 with Cr(CO)5 · THF yield Li(THF)2Et2O[Cr(CO)4{η2-(tBu2P)2P}η1-Cr(CO)5] 2 and the compounds [Cr(CO)4{η2-(tBu2P)2PH}] 3, [Cr(CO)5{η1-(tBu2P)2PH}] 4, (tBu2P)2PH 5 and tBu2PH · Cr(CO)5 6. The formation of 3, 4, 5 and 6 is due to byproducts coming from the synthesis of 1. 2 reacts with CH3COOH under formation of 3. After addition of 12-crown-4 1 with NBD · Cr(CO)4 in THF forms Li(12-crown-4)2[Cr(CO)4-{η2-(tBu2P)2P}] 7 (yellow crystals). 7 reacts with CH3COOH to 3 - which regenerates 7 with LiBu - with Cr(CO)5THF to compound 2, with NBD · Cr(CO)4 in THF to 2 and 3 (ratio 1 : 1). With EtBr, 7 forms [Cr(CO)4{η2-(tBu2P)2PEt}] 8, and [Cr(CO)4{η2-(tBu2P)2PBr}] 9 with BrCH2—CH2Br. The compounds were characterized by means of 1H, 13C, 31P, 7Li NMR spectroscopy, IR spectroscopy, elementary analysis, mass spectra, and 2, 3 and 4 additionally by means of X-ray diffraction analysis.2 crystallizes in the space group P1 with 2 formula units in the elementary cell; a = 10.137(9), b = 15.295(12), c = 15.897(14) Å; α = 101.82(7), β = 91.65(7), γ = 98.99(7)°; 3 crystallizes in the space group P2t/n with 4 molecules in the elementary unit; a = 11.914(6), b = 15.217(10), c = 14.534(10) Å; α = 90, β = 103.56(5), γ = 90°. 4: space group P1 with 2 molecules in the elementary unit; a = 8.844(4), b = 12.291(6), c = 14.411(7) Å, α = 66.55(2), β = 89.27(2), γ = 71.44(2)°.
    Notes: Umsetzungen von Li(THF)2[η2-(tBu2P)2P] 1 mit Cr(CO)5 · THF führen zum Li(THF)2Et2O[Cr(CO)4{η2-(tBu2P)2P}η1-Cr(CO)5] 2 sowie zu [Cr(CO)4{η2-(tBu2P)2PH}] 3, [Cr(CO)5{η1-(tBu2P)2PH}] 4, (tBu2P)2PH 5 und tBu2PH · Cr(CO)5 6, wobei die Bildung von 3, 4, 5 und 6 auf Nebenprodukte aus der Herstellung von 1 zurückgeht. 2 reagiert mit CH3COOH unter Bildung von 3. 1 bildet mit NBD · Cr(CO)4 in THF nach Zugabe von 12-Krone-4 das Li(12-Krone-4)2[Cr(CO)4{η2-(tBu2P)2P}] 7 (gelbe Kristalle). 7 reagiert mit CH3COOH zu 3 - aus dem sich mit LiBu Verbindung 7 zurückbildet -, mit Cr(CO)5THF zu Verbindung 2, mit NBD · Cr(CO)4 in THF zu 2 und 3 (Verhältnis 1 : 1). 7 bildet mit EtBr das [Cr(CO)4{η2-(tBu2P)2PEt}] 8, mit BrCH2—CH2Br das [Cr(CO)4{η2-(tBu2P)2PBr}] 9. Die Verbindungen wurden über ihre 1H-, 13C-, 31P-, 7Li-NMR-Spektren, IR-Spektren, Elementaranalysen und Massenspektren charakterisiert sowie 2, 3 und 4 durch Röntgenstrukturanalysen.2 kristallisiert in der Raumgruppe P1 mit 2 Formeleinheiten pro Elementarzelle; a = 10,137(9), b = 15,295 (12), c = 15,897(14) Å; α = 101,82(7), β = 91,65(7), γ = 98,99(7)°; 3 in Raumgruppe P21/n mit 4 Molekülen in der Elementarzelle; a = 11,914(6), b = 15,217(10), c = 14,534(10) Å; α = 90, β = 103,56(5), γ = 90°. 4 in Raumgruppe P1 mit 2 Molekülen pro Elementarzelle; a = 8,844(4), b = 12,291(6), c = 14,411(7) Å, α = 66,55(2), β = 89,27(2), γ = 71,44(2)°.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...