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
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 411-414 
    ISSN: 0009-2940
    Keywords: Phosphaalkyne, amino- ; [3 + 2] Cycloaddition ; 1,2,4-Diazaphospholes ; 1,2,3-Diazaphospholes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactive E = C(p - p)π Systems, XXXII[1].  -  First Representatives of Amino-Substituted 1,2,4-Diazaphospholes(Diisopropylamino)phosphaethyne iPr2N - C≡P reacts at 20° C in a [3 + 2] cycloaddition with (trifluoromethyl)diazomethane (2a) or methyl diazoacetate (2b) to yield a mixture of the corresponding regioisomers 1H-1,2,4-diazaphospholes (5a or 5b) and 1H-1,2,3-diazaphospholes (6a or 6b) in quantitative yields (isomer ratio: 5a/6a = 2:1; 5b/6b = 4:1). X-ray diffraction studies on 5a and 5b indicate a delicate charge balance in the bonding system of 1H-1,2,4,σ2-diazaphospholes under the influence of the exocyclic push/pull substituents iPr2N and CF3 or CO2Me, respectively.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 0009-2940
    Keywords: Selenium ; Fluorine ; Amides ; Cleavage reactions ; Cycloadditions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(trifluoromethylketiminoalkyl)diselanes [SeC(=NR)CF3]2 (6) [R = Me (a), iPr (b), tBu (c)] have been prepared in high yields (55-70%) by reaction of the diselane (SeC2F5)2 (2) with RNH2. However, the analogous reaction of 2 with secondary amines, R2NH, results in the cleavage of the Se-Se bond and leads to the N,N-dialkyl-2,2,2-trifluoroselenoacetamides Se=C(NR2)CF3 (7) [R = Me (a), iPr (b)]. Cleavage of 6a-6c with Me3SnH affords the selenoamides Se=C(NHR)CF3 (9) and the corresponding stannylselanes Me3SnSeC(=NR)CF3 (10) [R = Me(a), iPr (b), tBu (c)]. Selenoamides 7 and 9 can also be prepared from pentafluoroethylselenol HSeC2F5 (3), Se=C(F)CF3, (1) or its polymer [SeC(F)CF3]n (4) and primary or secondary amines. N,N-dialkyl-2-methyl-3-fluoro-4,4,4-trifluoroselenoacrylamides Se=C(NR2)C(Me)=C(F)CF3[R = Et (13a), iPr (13b)] are prepared in moderate yields under mild conditions by treating either trifluoromethylselenocarbonyl fluoride (1) or its polymer [SeC(F)CF3]n with 1-dialkylamino-1-propynes. The reaction proceeds by [2 + 2] cycloaddition and stereospecific electrocyclic ring-opening, yielding, with respect to the resulting C=C double bond, the E isomer as the only product. The molecular structures of 7b, 9a and 13b show the typical features of selenoamides with C(Se)-N bond shortening and C-Se bond elongation due to π interaction of the N lone pair with the C=Se double bond. The observed perpendicular orientation of the selenoamide and the alkene units of 13b prevents π delocalization.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 3
    ISSN: 0044-2313
    Keywords: Selenium ; bromoselenates(II) ; preparation ; crystal structure ; FIR spectra ; Raman spectra ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis, Structure, and Properties of the Novel Bromoselenates(II) [Se3Br8]2-, [Se4Br14]2-, and [Se5Br12]2-. Crystal Structures of [Cu(i-PropCN)4]2[Se3Br8], [EtPh3P]2[Se4Br14], and [n-Prop4N]2[Se5Br12]Using the symproportionation of elemental selenium and selenium tetrabromide in polar aprotic solvents a new class of tri-, tetra-, and pentanuclear bromoselenates(II) was obtained. In 2-methylpropionitrile solution the novel ion [Se3Br8]2- was stabilized and isolated as its black solvated copper salt. The crystals of [Cu(i-PropCN)4]2[Se3Br8] are monoclinic (C 2/c, a = 20.753(6), b = 13.344(4), c = 19.149(6) Å, β = 90.09(3)° at 140K, Z = 4) and contain trigonal star-shaped ions [Se3Br8]2- consisting of three edge-sharing square planar SeBr4 units. The mean terminal and μ3-bridging Se—Br bond lengths are 2.408 Å, respectively. [EtPh3P]2[Se4Br14] was obtained from dichloromethane solutions as dark red square-shaped crystals. The X-ray structure analysis (space group P 21/n, a = 11.400(3), b = 11.815(3), c = 20.720(A) Å, β = 92.50(3)° at 140 K, Z = 2) shows the crystals to contain tetranuclear ions [Se4Br14]2- that are built of two parallel planar [Se2Br6] units connected via two linear μBr-bridges. In the interesting delocalized electronic system a formal oxidation number of +1 has to be assigned to the bridging bromine. The mean terminal Se—Br bond length is 2.411 Å, the bridging bond lengths are 2.764 Å in the planar Se2Br6 units 2.594 Å in the linear Se—Br—Se bridges. Dark red [n-Prop4N]2[Se5Br12] was also isolated from CH2Cl2 solutions. It crystallizes in the tetragonal space group P 42/mnm (a = 14.798(3), c = 11.69(2) Å at 140 K, Z = 2) and its structure shows the novel pentanuclear ion [se5Br12]2-, consisting of a central square planar SeBr4 unit with two of its trans-edges being shared with additional pairs of square planar SeBr4, units. The anion can be described as two star-like Se3Br8 fragments with one sharing Se. The mean terminal and μ3-bridging Se—Br bond lengths are 2.343 Å and 2.956 Å, respectively. The vibrational spectra of the novel anions are reported and discussed.
    Notes: Durch Symproportionierung von elementarem Selen und Selentetrabromid in polaren protischen Lösungsmitteln wurde eine neue Klasse tri-, tetra- und pentanuklearer Bromoselenate(II) dargestellt. In 2-Methylpropionitril als Lösungsmittel wurde das strukturell neuartige Ion [Se3Br8]2- stabilisiert und als schwarzes solvatisiertes Kupfersalz isoliert. Kristalle von [Cu(i-PropCN)4]2[Se3Br8] sind monoklin (C2/c, a = 20,753(6), b = 13,344(4), c = 19,149(6) Å, β = 90,09(3)° bei 140K, Z = 4) und enthalten trigonale sternförmige Ionen [Se3Br8]2-, die aus drei kantenverknüpften quadratisch-planaren SeBr4-Einheiten bestehen. Die mittleren endständigen und μ3-verbrückenden Se—Br-Bindungslängen betragen 2,408 Å und 2,911 Å. [EtPh3P]2[Se4Br14] wurde aus Lösungen in Dichlormethan in Form dunkelroter Kristalle erhalten. Wie die Röntgenstrukturanalyse zeigt (Raumgruppe P21/n, a = 11,400(3), b = 11,815(3), c = 20,720(7) Å, β = 92,50(3)° bei 140K, Z = 2), enthalten sie vierkernige Ionen [Se4Br14]2-, die aus zwei parallel angeordneten, über lineare μBr-Brücken verknüpften Se2Br6-Einheiten aufgebaut sind. In diesem bemerkenswerten delokalisierten Elektronensystem muβ für das verbrückende Brom die formale Oxidationszahl + 1 angenommen werden. Die mittlere Se—Brterm-Bindungslängen sind 2,411 Å, die Brückenbindungslängen 2,764 Å in den planaren Se2Br6-Einheiten sowie 2,594 Å in den linearen Se—Br—Se-Brücken. Dunkelrotes [n-Prop4N]2[Se5Br12] konnte ebenfalls aus Lösungen in CH2Cl2 dargestellt werden. Es kristallisiert tetragonal (Raumgruppe P42/mnm, a = 14,798(3), c = 11,169(2) Å bei 140K, Z = 2). Seine Struktur enthält neuartige molekulare Ionen [Se5Br12]2-, die aus einer zentralen quadratisch-planaren SeBr4-Einheit bestehen, die über zwei trans-Kanten mit jeweils zwei weiteren quadratisch-planaren SeBr4-Einheiten verknüpft ist. Das Anion kann als über ein Selenatom verknüpfte Anordnung zweier sternförmiger Se3Br8-Fragmente beschrieben werden. Die mittleren endständigen und μ3-verbrückenden Se—Br-Abstände sind 2,343 Å und 2,956 Å. Über schwingungsspektroskopische Untersuchungen der neuen Anionen wird berichtet.
    Additional Material: 7 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...