Tuning of magnetic exchange interactions between organic radicals through bond and space

dc.contributor.authorRavat, Prince
dc.date.accessioned2014-11-06T12:38:04Z
dc.date.available2014-11-06T13:38:04Z
dc.date.issued2014
dc.description.abstractThe dissertation entitled "Tuning of magnetic exchange interactions between organic radicals through bond and space" comprises eight chapters. In the initial part of chapter 1, an overview of organic radicals and their applications were discussed and in the latter part motivation and objective of thesis was described. As the EPR spectroscopy is a necessary tool to study organic radicals, the basic principles of EPR spectroscopy were discussed in chapter 2. rnAntiferromagnetically coupled species can be considered as a source of interacting bosons. Consequently, such biradicals can serve as molecular models of a gas of magnetic excitations which can be used for quantum computing or quantum information processing. Notably, initial small triplet state population in weakly AF coupled biradicals can be switched into larger in the presence of applied magnetic field. Such biradical systems are promising molecular models for studying the phenomena of magnetic field-induced Bose-Einstein condensation in the solid state. To observe such phenomena it is very important to control the intra- as well as inter-molecular magnetic exchange interactions. Chapters 3 to 5 deals with the tuning of intra- and inter-molecular exchange interactions utilizing different approaches. Some of which include changing the length of Ï -spacer, introduction of functional groups, metal complex formation with diamagnetic metal ion, variation of radical moieties etc. During this study I came across two very interesting molecules 2,7-TMPNO and BPNO, which exist in semi-quinoid form and exhibits characteristic of the biradical and quinoid form simultaneously. The 2,7-TMPNO possesses the singlet-triplet energy gap of Î EST = â 1185 K. So it is nearly unrealistic to observe the magnetic field induced spin switching. So we studied the spin switching of this molecule by photo-excitation which was discussed in chapter 6. The structural similarity of BPNO with Tschitschibabin- HC allowed us to dig the discrepancies related to ground state of Tschitschibabin- hydrocarbon(Discussed in chapter 7). Finally, in chapter 8 the synthesis and characterization of a neutral paramagnetic HBC derivative (HBCNO) is discussed. The magneto liquid crystalline properties of HBCNO were studied by DSC and EPR spectroscopy.rnen_GB
dc.identifier.doihttp://doi.org/10.25358/openscience-2913
dc.identifier.urihttps://openscience.ub.uni-mainz.de/handle/20.500.12030/2915
dc.identifier.urnurn:nbn:de:hebis:77-38892
dc.language.isoeng
dc.rightsInC-1.0de_DE
dc.rights.urihttps://rightsstatements.org/vocab/InC/1.0/
dc.subject.ddc540 Chemiede_DE
dc.subject.ddc540 Chemistry and allied sciencesen_GB
dc.titleTuning of magnetic exchange interactions between organic radicals through bond and spaceen_GB
dc.typeDissertationde_DE
jgu.description.extent234 S.
jgu.organisation.departmentFB 09 Chemie, Pharmazie u. Geowissensch.
jgu.organisation.nameJohannes Gutenberg-Universität Mainz
jgu.organisation.number7950
jgu.organisation.placeMainz
jgu.organisation.rorhttps://ror.org/023b0x485
jgu.organisation.year2014
jgu.rights.accessrightsopenAccess
jgu.subject.ddccode540
jgu.type.dinitypePhDThesis
jgu.type.resourceText
jgu.type.versionOriginal worken_GB
opus.date.accessioned2014-11-06T12:38:04Z
opus.date.available2014-11-06T13:38:04
opus.date.modified2020-06-19T06:49:36Z
opus.identifier.opusid3889
opus.institute.number0906
opus.metadataonlyfalse
opus.organisation.stringFB 09: Chemie, Pharmazie und Geowissenschaften: Institut für Physikalische Chemiede_DE
opus.subject.dfgcode00-000
opus.type.contenttypeDissertationde_DE
opus.type.contenttypeDissertationen_GB

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