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  • Metalloboranes.  (1)
  • anthracene  (1)
  • 1
    Online-Ressource
    Online-Ressource
    Berlin, Heidelberg :Springer Berlin / Heidelberg,
    Schlagwort(e): Metalloboranes. ; Electronic books.
    Beschreibung / Inhaltsverzeichnis: With information that will remain valid for years, this series presents critical reviews of the present position and future trends in modern research into chemical structure and bonding. It features concise reports, each written by world-renowned experts.
    Materialart: Online-Ressource
    Seiten: 1 online resource (226 pages)
    Ausgabe: 1st ed.
    ISBN: 9783540786344
    Serie: Structure and Bonding Series ; v.130
    Sprache: Englisch
    Anmerkung: Intro -- Structure and Bonding -- Series Editor -- Volume Editors -- Editorial Board -- Structure and Bonding Also Available Electronically -- Preface -- Contents -- Transition Metal Borylene Complexes -- Transition Metal Boryl Complexes -- Transition Metal σ-Borane Complexes -- Coordination Modes and Hydride Exchange Dynamics in Transition Metal Tetrahydroborate Complexes -- Author Index Volumes 101-130 -- Subject Index.
    Standort Signatur Einschränkungen Verfügbarkeit
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  • 2
    Digitale Medien
    Digitale Medien
    New York, NY [u.a.] : Wiley-Blackwell
    Applied Organometallic Chemistry 10 (1996), S. 305-316 
    ISSN: 0268-2605
    Schlagwort(e): boron ; nonlinear optics ; third-order ; hyperpolarizability ; organic material ; fluorescence ; molecular structure ; benzene ; anthracene ; stilbene ; Chemistry ; Industrial Chemistry and Chemical Engineering
    Quelle: Wiley InterScience Backfile Collection 1832-2000
    Thema: Chemie und Pharmazie
    Notizen: The third-order nonlinear optical properties (second molecular hyperpolarizabilities, γ), of a series of organoboron compounds containing dimesitylboron moieties have been investigated by third harmonic generation (THG) measurements at 1.907 μm. Symmetric systems with B(mes)2 groups (mes=2,4,6-Me3C6H2) at both ends, e.g. (mes)2B-Y-B(mes)2 where Y=(C6H4)n (n=1,2) or trans-trans-CH=CH-(C6H4)n-CH=CH- (n=1,2), were prepared as well as push- pull systems of the form D-Y-B(mes)2 where D=MeS, Me2N, H2N, etc., and Y=C6H4, C6H4-C≅C-, C6H4-CH=CH-, C6H4-CH=CH-C6H4. The B(mes)2 group compares favorably with the more commonly used NO2 acceptor function for enhancing γ. Values of γ increase significantly with increasing length of π-conjugation for both symmetric and unsymmetric molecules. The MeS group is much more efficient than MeO for enhancing γ. Values as high as 22910-36 esu are reported for trans-trans-(mes)2-B-CH=CH-(C6H4)2-CH=CH-B(mes)2 which has a lmax for absorption of 370 nm. Crystal and molecular structures of the bis(dimesitylboryl) benzene and anthracene compounds 1,4-C6H4-{B(mes)2}2 and 9,10-C14H8{B(mes)2}2 are reported, as are fluorescence maxima for the symmetric molecules.
    Zusätzliches Material: 4 Ill.
    Materialart: Digitale Medien
    Standort Signatur Einschränkungen Verfügbarkeit
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