Library

X
feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 2000-2004  (3)
Source
Material
Years
Year
  • 1
    Electronic Resource
    Electronic Resource
    A donor–acceptor adduct: sterically encumbered terphenyl dichloro[2,6-bis(2,4,6-triisopropylphenyl)phenyl]dichloro(pyridine)gallium benzene hemisolvate (2001)
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m88-m91 
    Details
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The molecular structure of the benzene-solvated donor–acceptor complex dichloro[2,2′′,4,4′′,6,6′′-hexaisopropyl-1,1′:3′,1′′-terphenyl-C2′](pyridine)gallium benzene hemisolvate, henceforth known as 2,6-Trip2-C6H3GaCl2-pyridine benzene hemisolvate or (1) + 0.5 C6H6 (Trip = 2,4,6-triisopropylphenyl), [GaCl2(C36H49)(C5H5N)]·0.5C6H6, has been determined. The asymmetric unit consists of four independent molecules of (1) and two benzene solvent molecules. The Ga—C, Ga—N and Ga—Cl bond lengths span the ranges 1.979 (7)–1.983 (2), 2.028 (6)–2.040 (7) and 2.179 (2)–2.212 (2) Å, respectively. All independent molecules of (1) have essentially the same geometry with slight differences in the orientation of the peripheral phenyl rings and isopropyl groups in the terphenyl moiety.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1107/S1600536801001787
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 2
    Electronic Resource
    Electronic Resource
    A primary monomeric alane: [N,N′-bis(2,6-diisopropylphenyl)pentane-2,4-diiminato-N,N′]dihydridoaluminium (2001)
    Copenhagen : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. m227-m228 
    Details
    ISSN: 1600-5368
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title compound, [AlH2(C29H41N2)], is an example of a sterically encumbered monomeric primary alane. The bond lengths are within normal ranges. The N—Al distance is 1.8989 (12) Å. The H atoms bonded to the aluminium center were located in a difference map and refined to Al—H distances of 1.51 (2) and 1.518 (19) Å. There are no significant intermolecular interactions.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1107/S1600536801007413
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
    Paper (German National Licenses)
    Fulltext
  • 3
    Electronic Resource
    Electronic Resource
    A terphenyl halide series: 2,6-Trip2H3C6X (Trip = 2,4,6-triisopropylphenyl; X = Cl, Br, I) (2000)
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e514-e515 
    Details
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The sterically encumbered terphenyl halides 2′-chloro-2,2′′,4,4′′,6,6′′-hexaisopropyl-1,1′:3′,1′′-terphenyl, C36H49Cl, (I), 2′-bromo-2,2′′,4,4′′,6,6′′-hexaisopropyl-1,1′:3′,1′′-terphenyl, C36H49Br, (II), and 2′-iodo-2,2′′,4,4′′,6,6′′-hexaisopropyl-1,1′:3′,1′′-terphenyl, C36H49I, (III), crystallize in space group Pnma. They are isomorphous and isostructural with a plane of symmetry through the centre of the molecule. The C–halide bond distances are 1.745 (3), 1.910 (4) and 2.102 (6) Å for (I)–(III), respectively.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1107/S0108270100013020
    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...