120517-37-5Relevant articles and documents
Synthesis of nanometer-sized homo- and heteroorganometallic tripodaphyrins
Mongin, Olivier,Gossauer, Albert
, p. 6835 - 6846 (1997)
Tripodaphyrins are tetrahedral or pyramidal assemblies in which a porphyrin macrocycle situated on the top of the molecule is 'supported' by three 'legs' consisting of linear arrays of covalently linked rigid constitutive elements. The edge-length at the 'base' of the molecules which have been synthesized until now lies in the range from 3.2 to 6.5 nm. In some tripodaphyrins (3a-c) the chromophore situated on the top of the molecule differs on the complexed metal ion from the other three, which are located at the ends of the 'legs'. Owing to the dimensions of the molecules, no intramolecular interaction between the chronophores is observed, even in the presence of a paramagnetic Cu(II) chelate.
Convenient synthesis of green diisoindolodithienylpyrromethene-dialkynyl borane dyes
Goeb, Sebastien,Ziessel, Raymond
, p. 737 - 740 (2007)
(Graph Presented) Versatile dyes based on diisoindolodithienylpyrromethene substituted at the boron center by alkynylaryl chromophores have been developed that efficiently fluorescence in the near infrared. Fast intramolecular energy transfer from the appended alkynyl units to the central core provides Stokes shifts above 16 000 cm-1.
STRUCTURE, SYNTHESIS, AND APPLICATIONS FOR OLIGO PHENYLENE ETHYNYLENES (OPES)
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Page/Page column 3, (2012/02/02)
The present disclosure provides novel oligo phenylene ethynylene (OPE) compounds, methods for synthesizing these compounds, and materials and substances incorporating these compounds. The various OPEs show antibacterial, antiviral and antifungal activity.