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Sökning: onr:"swepub:oai:DiVA.org:liu-132781" > Synthesis and spect...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00005048nam a2200493 4500
001oai:DiVA.org:liu-132781
003SwePub
008161124s2016 | |||||||||||000 ||eng|
020 a 9789176856253q print
024a https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-1327812 URI
024a https://doi.org/10.3384/lic.diva-1327812 DOI
040 a (SwePub)liu
041 a engb eng
042 9 SwePub
072 7a vet2 swepub-contenttype
072 7a lic2 swepub-publicationtype
100a Carlsson, Andreasu Linköpings universitet,Kemi,Tekniska fakulteten,Swedish National Forens Centre NFC, Linkoping, Sweden4 aut0 (Swepub:liu)andca72
2451 0a Synthesis and spectroscopic characterization of emerging synthetic cannabinoids and cathinones
264 1a Linköping :b Linköping University Electronic Press,c 2016
300 a 62 s.
338 a electronic2 rdacarrier
490a Linköping Studies in Science and Technology. Thesis,x 0280-7971 ;v 1766
520 a The application of different analytical techniques is fundamental in forensic drug analysis. In the wake of the occurrence of large numbers of new psychoactive substances possessing similar chemical structures as already known ones, focus has been placed on applied criteria for their univocal identification. These criteria vary, obviously, depending on the applied technique and analytical approach. However, when two or more substances are proven to have similar analytical properties, these criteria no longer apply, which imply that complementary techniques have to be used in their differentiation.This work describes the synthesis of some structural analogues to synthetic cannabinoids and cathinones based on the evolving patterns in the illicit drug market. Six synthetic cannabinoids and six synthetic cathinones were synthesized, that, at the time for this study, were not as yet found in drug seizures. Further, a selection of their spectroscopic data is compared to those of already existing analogues; mainly isomers and homologues. The applied techniques were mass spectrometry (MS), Fourier transformed infrared (FTIR, gas phase) spectroscopy and nuclear magnetic resonance (NMR) spectroscopy. In total, 59 different compounds were analyzed with the  selected techniques.The results from comparison of spectroscopic data showed that isomeric substances may in some cases be difficult to unambiguously identify based only on their GC-MS EI spectra. On the other hand, GC-FTIR demonstrated more distinguishable spectra. The spectra for the homologous compounds showed however, that the GC-FTIR technique was less successful compared to GC-MS. Also a pronounced fragmentation pattern for some of the cathinones was found.In conclusion, this thesis highlights the importance of using complementary techniques for the univocal identification of synthetic cannabinoids and cathinones. By increasing the number of analogues investigated, the more may be learnt about the capabilities of different techniques for structural differentiations, and thereby providing important identification criteria leading to trustworthy forensic evidence.
650 7a NATURVETENSKAPx Kemix Organisk kemi0 (SwePub)104052 hsv//swe
650 7a NATURAL SCIENCESx Chemical Sciencesx Organic Chemistry0 (SwePub)104052 hsv//eng
650 7a NATURVETENSKAPx Kemix Analytisk kemi0 (SwePub)104012 hsv//swe
650 7a NATURAL SCIENCESx Chemical Sciencesx Analytical Chemistry0 (SwePub)104012 hsv//eng
650 7a NATURVETENSKAPx Kemix Materialkemi0 (SwePub)104032 hsv//swe
650 7a NATURAL SCIENCESx Chemical Sciencesx Materials Chemistry0 (SwePub)104032 hsv//eng
650 7a NATURVETENSKAPx Fysikx Atom- och molekylfysik och optik0 (SwePub)103022 hsv//swe
650 7a NATURAL SCIENCESx Physical Sciencesx Atom and Molecular Physics and Optics0 (SwePub)103022 hsv//eng
700a Dahlén, Johan,c Dr.u Linköpings universitet,Kemi,Tekniska fakulteten4 ths0 (Swepub:liu)johda32
700a Josefsson, Martin,c Dr.u Linköpings universitet,Kemi,Tekniska fakulteten4 ths0 (Swepub:liu)marjo13
700a Konradsson, Peter,c Professoru Linköpings universitet,Kemi,Tekniska fakulteten4 ths0 (Swepub:liu)petko14
700a Dunne, Simon,c Dr.u Swedish National Forens Centre NFC, Linkoping, Sweden4 ths
700a Hedeland, Mikael,c Professoru Swedish National Veterinary Institute, Uppsala4 opn
710a Linköpings universitetb Kemi4 org
856u https://doi.org/10.3384/lic.diva-132781y Fulltext
856u https://liu.diva-portal.org/smash/get/diva2:1049312/FULLTEXT01.pdfx primaryx Raw objecty fulltext
856u https://liu.diva-portal.org/smash/get/diva2:1049312/COVER01.pdfy cover
856u https://liu.diva-portal.org/smash/get/diva2:1049312/PREVIEW01.jpgx Previewy preview image
856u http://liu.diva-portal.org/smash/get/diva2:1049312/FULLTEXT01
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:liu:diva-132781
8564 8u https://doi.org/10.3384/lic.diva-132781

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