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Synthesis and optical characterisation of platinum(II) poly-yne polymers incorporating substituted 1,4-diethynylbenzene derivatives and an investigation of the intermolecular interactions in the diethynylbenzene molecular precursors

Titelangaben

Khan, Muhammad S. ; Al-Mandhary, Muna R. A. ; Al-Suti, Mohammed K. ; Corcoran, Timothy C. ; Al-Mahrooqi, Yaqoub ; Attfield, J. Paul ; Feeder, Neil ; David, William I. F. ; Shankland, Kenneth ; Friend, Richard H. ; Köhler, Anna ; Marseglia, Elizabeth A. ; Tedesco, Emilio ; Tang, Chiu C. ; Raithby, Paul R. ; Collings, Jonathan C. ; Roscoe, Karl P. ; Batsanov, Andrei S. ; Stimson, Lorna M. ; Marder, Todd B.:
Synthesis and optical characterisation of platinum(II) poly-yne polymers incorporating substituted 1,4-diethynylbenzene derivatives and an investigation of the intermolecular interactions in the diethynylbenzene molecular precursors.
In: New Journal of Chemistry. Bd. 27 (2003) Heft 1 . - S. 140-149.
ISSN 1369-9261
DOI: https://doi.org/10.1039/B206946F

Abstract

A series of 1,4-diethynylbenzene (1) derivatives, H–C[triple bond, length as m-dash]C–R–C[triple bond, length as m-dash]C–H with R = C6H3NH2 (2), C6H3F (3), C6H2F2-2,5 (4), C6F4 (5), C6H2(OCH3)2-2,5 (6) and C6H2(OnC8H17)2-2,5 (7) has been synthesised and their crystal structures determined by single crystal (2–5) or powder (6, 7) X-ray diffraction. The C[triple bond, length as m-dash]CHπC[triple bond, length as m-dash]C hydrogen bonds dominating structure 1 are gradually replaced by C[triple bond, length as m-dash]C–HF ones with the increase of fluorination (3 → 5), or completely replaced by C[triple bond, length as m-dash]CHN and NHπC[triple bond, length as m-dash]C bonds in 2, and C[triple bond, length as m-dash]CHO in 6 and 7. The related platinum-based polymers, trans-[–Pt(PnBu3)2–C[triple bond, length as m-dash]C–R–C[triple bond, length as m-dash]C–]n (R = as above and C6H4,) have been prepared and characterised by spectroscopic methods and thermogravimetry, which show that the amino- and methoxy-derivatives have lowest thermal stability while the fluorinated ones exhibit increasing thermal stability with increasing fluorination. Optical spectroscopic measurements reveal that substituents on the aromatic spacer group do not create strong donor–acceptor interactions along the rigid backbone of the organometallic polymers.

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Publikationsform: Artikel in einer Zeitschrift
Begutachteter Beitrag: Nein
Institutionen der Universität: Fakultäten > Fakultät für Mathematik, Physik und Informatik > Physikalisches Institut > Lehrstuhl Experimentalphysik II - Optoelektronik weicher Materie > Lehrstuhl Experimentalphysik II - Optoelektronik weicher Materie - Univ.-Prof. Dr. Anna Köhler
Fakultäten
Fakultäten > Fakultät für Mathematik, Physik und Informatik
Fakultäten > Fakultät für Mathematik, Physik und Informatik > Physikalisches Institut
Fakultäten > Fakultät für Mathematik, Physik und Informatik > Physikalisches Institut > Lehrstuhl Experimentalphysik II - Optoelektronik weicher Materie
Titel an der UBT entstanden: Nein
Themengebiete aus DDC: 500 Naturwissenschaften und Mathematik > 530 Physik
Eingestellt am: 18 Mär 2015 08:41
Letzte Änderung: 18 Mär 2015 08:41
URI: https://eref.uni-bayreuth.de/id/eprint/8465