http://rdf.ncbi.nlm.nih.gov/pubchem/patent/SK-277824-B6

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1d73b30001e07f53675a946996c96393
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C49-76
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07F11-00
filingDate 1990-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9619b288c707cd4410caed4943b35ccf
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2e8d30cb8bedf79315fc20d4baba5280
publicationDate 1995-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber SK-277824-B6
titleOfInvention Method of preparation of arenetricarbonyle complexes of chromium
abstract Solution is concerning the preparation of arenetricarbonyle complexes of chromium from hexacarbonyleochromium and respective aromatic compound which can be the benzene derivatives with substituens as alkyl, aryl, alkenyl, halogen, acyl, alkoxy, alkylthio, amino, alkyl or dialkyl amino, alkoxycarbonyl or polycyclic aromatic compounds as naphthalene, phenanthrene, acenaphthene, flourene atc. The essence of solution lies in fact, that the aromatic compound has an effect on hexa carbonyl chromium at boiling tempereture in solvent for example the satureted hydrocarbon, mixture of saturated hydrocarbons or Di-N-butylether at bath temperature 180 to 220 degrees of Celsius with adding 0,1 to 100 per cent volume of ester of carboxylic acid, at which per cent volume refere to volume of solvent. As esters are used methyl,- ethyl-n-butyl or n-pentylesters of formic acid, acetic acid, propionic or butyric acid.
priorityDate 1990-03-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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