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Modulation of Molecular Properties: Host–Guest Interactions for Structural Analysis and Chemical Reactions
Uppsala universitet, Teknisk-naturvetenskapliga vetenskapsområdet, Kemiska sektionen, Institutionen för kemi - BMC, Syntetisk organisk kemi.
2013 (engelsk)Doktoravhandling, med artikler (Annet vitenskapelig)
Abstract [en]

This thesis concerns the construction, use and modulation of various host–guest systems, from small bispidines for binding of inorganic ions to bisporphyrin clips for supramolecular systems.

Small flexible molecules undergo fast conformational movements when in solution. These conformational movements generate time-averaged population-weighted chemical shifts, coupling constants and NOEs when analysed by NMR spectroscopy. A bisporphyrin clip was designed to be used as a host for restriction of conformational movements of small flexible molecules by ditopic metal-ligand binding. Based on conformational analysis in combination with NMR analysis of molecular flexibility in solution (NAMFIS), the relative stereochemistry of flexible alditol-derived diamines containing three or four consecutive stereocentres could be determined.

To further explore the idea of conformational deconvolution via host–guest binding, two flexible molecular tweezers with photoswitchable moieties were developed. Upon photoswitching cis/trans isomerisation facilitates the opening and closing of these bisporphyrin hosts. A guest molecule could then be exposed to a “catch and stretch” or “catch and release” effect. Preliminary studies have shown that photoisomerisation of the constructed systems is possible without photodecomposition and preliminary binding studies have been conducted.

Controlled modulation of molecular conformations is of interest especially if the conformational steering activates a unit working as a nucleator in a larger structure or facilitates a reaction. The protonation-triggered modulation of bispidine conformations has been investigated. In addition to previously reported conformations we have observed that upon diprotonation a bispidine derivative can be driven into the unusual boat-boat conformation.

Finally, the unexpected formation of persistent organic radicals with a cyclophane motif from the reaction of N,N´-diphenyl-1-5-diazacyclooctane and AgBF4 is described. Interestingly, these diradicals exhibit features such as intramolecular π-stacking without lateral displacement and also intramolecular spin pairing.

 

sted, utgiver, år, opplag, sider
Uppsala: Acta Universitatis Upsaliensis, 2013. , s. 61
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, ISSN 1651-6214 ; 1070
Emneord [en]
host-guest systems, conformational analysis, NMR spectroscopy, bispidines, porphyrins
HSV kategori
Forskningsprogram
Kemi med inriktning mot organisk kemi
Identifikatorer
URN: urn:nbn:se:uu:diva-207138ISBN: 978-91-554-8747-8 (tryckt)OAI: oai:DiVA.org:uu-207138DiVA, id: diva2:646893
Disputas
2013-10-25, B41, BMC, Husargatan 3, Uppsala, 09:30 (engelsk)
Opponent
Veileder
Tilgjengelig fra: 2013-10-03 Laget: 2013-09-09 Sist oppdatert: 2014-01-23
Delarbeid
1. Conformational restriction of flexible molecules in solution by a semirigid bis-porphyrin molecular tweezer
Åpne denne publikasjonen i ny fane eller vindu >>Conformational restriction of flexible molecules in solution by a semirigid bis-porphyrin molecular tweezer
Vise andre…
2013 (engelsk)Inngår i: Tetrahedron, ISSN 0040-4020, E-ISSN 1464-5416, Vol. 69, nr 34, s. 7131-7138Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

A semirigid bis-porphyrin molecular clip with a glycoluril backbone has been synthesized. The clip provides an adaptable molecular cavity for binding of diamines. Binding constants for diamines of 104–107 M−1 are orders of magnitude higher than those for monoamines of 103 M−1, indicating a preference to bidentate binding. NMR studies confirmed that binding of bidentate guests occurs inside the clip. Short- and medium-size acyclic molecular guests are locked into a single, extended conformation, and also guests with longer flexible chains exhibit considerably less conformational mobility than when free in solution. The size of the cavity adapts to the guest size, as indicated by modelling studies and self diffusion constants of the complexes.

Emneord
Conformational analysis, NMR spectroscopy, Hosteguest systems, Supramolecular chemistry, Porphyrinoids
HSV kategori
Forskningsprogram
Kemi med inriktning mot organisk kemi
Identifikatorer
urn:nbn:se:uu:diva-206036 (URN)10.1016/j.tet.2013.06.013 (DOI)000322098000027 ()
Forskningsfinansiär
Swedish Research Council
Tilgjengelig fra: 2013-08-26 Laget: 2013-08-26 Sist oppdatert: 2017-12-06bibliografisk kontrollert
2. Improved stereochemical analysis of conformationally flexible diamines by binding to a bisporphyrin molecular clip
Åpne denne publikasjonen i ny fane eller vindu >>Improved stereochemical analysis of conformationally flexible diamines by binding to a bisporphyrin molecular clip
2013 (engelsk)Inngår i: Chemistry - A European Journal, ISSN 0947-6539, E-ISSN 1521-3765, Vol. 19, nr 43, s. 14631-14638Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

The relative stereochemistry of acyclic diamines with several stereogenic centers has been analyzed by NMR spectroscopy in combination with conformational deconvolution. Binding to a bisporphyrin molecular clip improves the stereochemical assignment significantly. The diamines were synthesized from inexpensive sugar alcohols, and their stable hydrochlorides were quantitatively converted into free bases by treatment with ion-exchange resin.

Emneord
configuration determination, conformational analysis, host–guest systems, N ligands, NMR spectroscopy
HSV kategori
Forskningsprogram
Organisk kemi
Identifikatorer
urn:nbn:se:uu:diva-206040 (URN)10.1002/chem.201300533 (DOI)000330288400025 ()
Forskningsfinansiär
Swedish Research Council
Tilgjengelig fra: 2013-08-26 Laget: 2013-08-26 Sist oppdatert: 2017-12-06bibliografisk kontrollert
3. Photomodulable bis-porphyrin molecular tweezers for conformational studies of diamine guests
Åpne denne publikasjonen i ny fane eller vindu >>Photomodulable bis-porphyrin molecular tweezers for conformational studies of diamine guests
Vise andre…
(engelsk)Manuskript (preprint) (Annet vitenskapelig)
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-206039 (URN)
Tilgjengelig fra: 2013-08-26 Laget: 2013-08-26 Sist oppdatert: 2014-01-23
4. Protonation-triggered Conformational Modulation of an N,N´‑Dialkylbispidine: First observation of the elusive boat-boat conformer
Åpne denne publikasjonen i ny fane eller vindu >>Protonation-triggered Conformational Modulation of an N,N´‑Dialkylbispidine: First observation of the elusive boat-boat conformer
2013 (engelsk)Inngår i: Organic and biomolecular chemistry, ISSN 1477-0520, E-ISSN 1477-0539, Vol. 11, s. 6292-6299Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Modulation of the solution conformations of N,N′-bis(benzhydryl)bispidine has been achieved by protonation. Conformers have been characterized by NMR spectroscopy using nuclear Overhauser effects and residual dipolar couplings. In contrast to the preference for the chair–chair conformation for the free base and the monoprotonated species, the diprotonated bispidine is revealed to exist as a mixture of chair–boat and boat–boat conformers. While boat–boat conformers of bispidines have previously not been detected, they are here observed to constitute up to 70% of the bispidine population.

HSV kategori
Forskningsprogram
Organisk kemi
Identifikatorer
urn:nbn:se:uu:diva-206042 (URN)10.1039/c3ob41122b (DOI)000324507100010 ()
Forskningsfinansiär
Swedish Research Council
Tilgjengelig fra: 2013-08-26 Laget: 2013-08-26 Sist oppdatert: 2017-12-06bibliografisk kontrollert
5. Synthesis of persistent organic dication diradicals incorporating a cyclophane motif with intramolecular pi-stacking
Åpne denne publikasjonen i ny fane eller vindu >>Synthesis of persistent organic dication diradicals incorporating a cyclophane motif with intramolecular pi-stacking
Vise andre…
(engelsk)Artikkel i tidsskrift (Annet vitenskapelig) Submitted
HSV kategori
Identifikatorer
urn:nbn:se:uu:diva-206043 (URN)
Tilgjengelig fra: 2013-08-26 Laget: 2013-08-26 Sist oppdatert: 2014-01-23bibliografisk kontrollert

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