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Search for "luminescence" in Full Text gives 127 result(s) in Beilstein Journal of Organic Chemistry.

Ring opening metathesis polymerization-derived block copolymers bearing chelating ligands: synthesis, metal immobilization and use in hydroformylation under micellar conditions

  • Gajanan M. Pawar,
  • Jochen Weckesser,
  • Siegfried Blechert and
  • Michael R. Buchmeiser

Beilstein J. Org. Chem. 2010, 6, No. 28, doi:10.3762/bjoc.6.28

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  • was performed using a Perkin-Elmer luminescence spectrometer LS50B. IR spectra were recorded on a Bruker Vector 22 using ATR technology. Elemental analysis was carried out on Elementar Varia El (Analytik Jena). GC-MS investigations were carried out on a Shimadzu GCMS-QP5050 with an AOC-20i Autosampler
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Published 23 Mar 2010

Functional properties of metallomesogens modulated by molecular and supramolecular exotic arrangements

  • Alessandra Crispini,
  • Mauro Ghedini and
  • Daniela Pucci

Beilstein J. Org. Chem. 2009, 5, No. 54, doi:10.3762/bjoc.5.54

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  • materials with more and more challenging requirements such as improved charge transport, luminescence, chirality and biological functions for high-tech applications has been directed towards the use of new mesomorphic systems [1][2][3][4][5][6][7][8][9][10][11][12][13][14]. Design principles based only on
  • -one) as a cyclometallating ligand and from the suitably functionalized curcumin β-diketonate as a complementary O,O chelating ligand (Figure 1). The presence of the principal ligand [39][40][41][42][43][44] introduces interesting luminescence properties into the metallic system (which is luminescent
  • organized into columns, the broad thermal stability and the luminescence in the red region of the visible spectrum make this new Pd(II) complex a very intriguing candidate for applications in OLED devices. A further class of ortho-palladated complexes has been obtained starting from the 2-phenylquinoline, a
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Published 12 Oct 2009
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