http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2010127788-A

Outgoing Links

Predicate Object
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C01B31-00
filingDate 2010-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2012-01-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2010127788-A
titleOfInvention AMINOFULLERENES AND METHOD FOR PRODUCING THEM
abstract 1. Aminofullerenes of the general formula 1, namely:! ! where is X, but is not limited to:! - a negative charge ("-") localized on the fullerene frame, or! - a chlorine atom (-Cl) attached to the carbon frame, or! - a nitro group (-NO2) or a nitrate group (-ONO2) attached to a carbon skeleton, or! - a hydrogen atom (-H), a linear or branched alkyl (CnH2n + 1; n = 1-20), alkenyl (CnH2n-1; n = 1-20) or alkynyl radical (CnH2n-3; n = 1-20) attached to the fullerene framework, or! - alkoxyl OR or thiolate fragment of SR attached to the fullerene backbone, where R is a hydrogen atom or a linear or branched alkyl (CnH2n + 1; n = 1-20), alkenyl (CnH2n-1; n = 1-20) or alkynyl radical (CnH2n-3; n = 1-20), or! - the remainder of the thio acid -S (CH2) nCOOH or its ester -S (CH2) nCOOR, or the amide -S (CH2) nCONR1R2 attached to the fullerene backbone, where n = 1-20, and R, R1 and R2 are hydrogen atoms or linear or branched alkyl (CmH2m + 1; n = 1-20), alkenyl (CmH2m-1; n = 1-20) or alkynyl (CmH2m-3; n = 1-20) radicals; ! where the NR1R2 fragment is selected from the group, but is not limited to the following definitions:! is the amine residue, where R1 and R2 are hydrogen atoms or linear or branched alkyl (CmH2m + 1; n = 1-20), alkenyl (CmH2m-1; n = 1-20) or alkynyl radicals (CmH2m-3; n = 1-20); ! - residues of aliphatic alcohols - (CH2) nOH, ethers - (CH2) nOR'1 and - (CH2CH2O) nR'1, thiols - (CH2) nSH, acids - (CH2) nCOOH, their esters - (CH2) nCOOR '1 or amides - (CH2) nCONR'1R'2, for which n = 0-20, and R'1 and R'2 are hydrogen atoms or linear or branched alkyl (CmH2m + 1; n = 1-20) alkenyl (CmH2m-1; n = 1-20) or alkynyl radicals (CmH2m-3; n = 1-20); ! - fragments of the general formula -NH- * CH (R'1) (CH2) nCOX, regardless of the spatial configuration of the substituents at the chiral center * C (D and L enantiomers and racemic ph
priorityDate 2010-07-07-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID71077
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419488910
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID426100952
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID25076
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID455585947
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419483812
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5950
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID104822
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6267
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558042
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419484026
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419527708
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9060
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4837
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23657811
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6137
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419485715
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419487901
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419549088
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6140
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID750
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID943
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559194
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5862
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID415061053
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6287
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419538410
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6288
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419474137
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419550758
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419490523
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458392451
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6274
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419548780
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419546724
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419558427
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID457192620
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559581
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID458427722
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419537510
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6398619
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID33032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5961
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6057
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6106
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6306
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5960
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419555909
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419556475
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419490256
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419537453
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419539584

Total number of triples: 62.