UWSpace is currently experiencing technical difficulties resulting from its recent migration to a new version of its software. These technical issues are not affecting the submission and browse features of the site. UWaterloo community members may continue submitting items to UWSpace. We apologize for the inconvenience, and are actively working to resolve these technical issues.
 

Effects of Metal Cations and Cyclodextrins on 1,3 Diphenyltriazenes Isomerization and Decomposition

dc.comment.hiddencorrected editionen
dc.contributor.authorXu, Tingting
dc.date.accessioned2009-09-18T20:10:20Z
dc.date.available2009-09-18T20:10:20Z
dc.date.issued2009-09-18T20:10:20Z
dc.date.submitted2009-09-14
dc.description.abstractTriazenes are molecules characterized by having the triazeno group (–N=N–N<). They are known as photoactive molecules due to trans-cis photoinduced isomerization around the N=N bond. Their nucleophilic character makes them good ligands to metal centers. A study on the potential ability of photochromic organic ligand triazenes to undergo reversible cis-trans photoisomerization and, in turn, photoreversible complexation with metal cations was carried out in aqueous solutions. Metal-triazenide complexes are instantaneously formed upon addition of metal cations to trans-triazenes dissolved in aqueous solutions. For silver-triazenide and mercury-triazenide complexes, the metal-to-ligand ratios are 1:1 and 1:2, respectively. Unfortunately, target metal-triazenide complexes do not photoisomerize upon 355 nm laser excitation. Triazenes are also known to be unstable materials under acidic conditions. A study on the effects of cyclodextrins (CDs) on the rate of acid-catalyzed decomposition of 1,3-diphenyl-triazenes was carried out in 2% MeOH aqueous buffer solutions by means of spectroscopic methods. CDs inhibit triazenes decomposition through inclusion complex formation. The inclusion complexes render the guest triazene significantly less basic as a consequence of the less polar nature of the CD cavity (a microsolvent effect). For any given triazene, the inhibition effect is dependent on both the size of the cyclodextrin cavity and the substituents on the cavity rims. Binding constants for 1:1 host:guest complexes increase in the order α-CD < ß-CD ~ TM-ß-CD < HP-ß-CD; in the case of α CD, formation of 2:1 complexes is also observed.en
dc.identifier.urihttp://hdl.handle.net/10012/4708
dc.language.isoenen
dc.pendingfalseen
dc.publisherUniversity of Waterlooen
dc.subjecttriazeneen
dc.subjectcyclodextrinen
dc.subject.programChemistryen
dc.titleEffects of Metal Cations and Cyclodextrins on 1,3 Diphenyltriazenes Isomerization and Decompositionen
dc.typeMaster Thesisen
uws-etd.degreeMaster of Scienceen
uws-etd.degree.departmentChemistryen
uws.peerReviewStatusUnrevieweden
uws.scholarLevelGraduateen
uws.typeOfResourceTexten

Files

Original bundle
Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
Xu_Tingting.pdf
Size:
6.39 MB
Format:
Adobe Portable Document Format
License bundle
Now showing 1 - 1 of 1
No Thumbnail Available
Name:
license.txt
Size:
245 B
Format:
Item-specific license agreed upon to submission
Description:

Collections