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filingDate 1981-01-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1326d2ec0082e0f8f735a7c8abb0b835
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_96562308c02d4215ac5d86c2553a518a
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publicationDate 1981-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0032670-A1
titleOfInvention Light collector systems and the use of coumarin derivatives as energy converters in such systems
abstract T 0 oder NR 4 , wobei R 4 für Wasserstoff, gegebenenfalls substituiertes Alkyl oder gegebenenfalls substituiertes Aryl steht; R, ein über ein C-Atom gebundener carbo- oder heterocyclischer sauerstofffreier 5- oder 6gliedriger Ring oder ein über ein N-Atom gebundener 5- oder 6gliedriger heterocyclischer Ring, der zu einer durch die Cumarin-N-Heterocyclus-Bindung gelegten Achse rotationsunsymmetrisch ist, wobei die genannten 5-oder 6gliedrigen Ringe nicht-ionogene Substituenten tragen können und an sie ein gegebenenfalls substituierter Benzol- oder ein gegebenenfalls substituierter Naphthalinring ankondensiert sein kann; R 2 Wasserstoff, Alkyl, Cycloalkyl, Aralkyl, Aryl, wobei die genannten Kohlenwasserstoffreste substituiert sein können, R 3 Wasserstoff, Alkyl, Cycloalkyl, Aralkyl, Aryl oder einen Rest -OR s , -SO 2 R 5 , -SO 2 NHR 5 , -NHCOR 5 , Halogen oder COOR 5 bezeichnen, wobei R s für Alkyl, Cycloalkyl, Aralkyl oder Aryl steht, nsowie die Verwendung von Cumarinderivaten als Energiewandler in Lichtsammelsystemen.Light collection system, characterized in that it is a coumarin derivative of the formula contains in the T 0 or NR 4 , where R 4 represents hydrogen, optionally substituted alkyl or optionally substituted aryl; R, a carbo- or heterocyclic oxygen-free 5- or 6-membered ring bonded via a C atom, or a 5- or 6-membered heterocyclic ring bonded via an N atom, which is rotationally asymmetrical to an axis through the coumarin-N-heterocycle bond , said 5-membered or 6-membered rings being able to carry nonionic substituents and to which an optionally substituted benzene or an optionally substituted naphthalene ring may be fused; R 2 is hydrogen, alkyl, cycloalkyl, aralkyl, aryl, where the hydrocarbon radicals mentioned can be substituted, R 3 denotes hydrogen, alkyl, cycloalkyl, aralkyl, aryl or a radical -OR s , -SO 2 R 5 , -SO 2 NHR 5 , -NHCOR 5 , halogen or COOR 5 , where R s is alkyl, cycloalkyl, aralkyl or Aryl stands, and the use of coumarin derivatives as energy converters in light collection systems.
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