Novel tetrathiafulvalene derivatives and macrocycles with sugar units: Synthesis and characterization
Date of Publication
1998
Document Type
Dissertation
Degree Name
Doctor of Philosophy in Chemistry
Subject Categories
Chemistry
College
College of Science
Department/Unit
Chemistry
Thesis Adviser
Gerardo C. Janairo
Defense Panel Chair
Eric Camilo R. Punzalan
Defense Panel Member
Jaime Raul O. Janairo
Wyona C. Patalinghug
Anamy Ma. C. Paano
Nancy Lazaro Llanos
Abstract/Summary
Novel tetrathiafulvalene (TTF) derivatives an macrocycles containing glucose units were synthesized. TTF is an electron rich molecule capable of pi-pi interaction while glucose is polyhydroxylated and has the ability to form hydrogen bonds. The macrocycle synthesis involves the stepwise deprotection of cyanoethyl protected TTF, reaction with acetylated dihaloglucose, followed by hydrolysis.
Abstract Format
html
Language
English
Format
Accession Number
TG02780
Shelf Location
Archives, The Learning Commons, 12F Henry Sy Sr. Hall
Physical Description
145 numb. leaves
Keywords
Chemical reactions; Derivatization; Sugar--Inversion; Hydrolysis; Biosynthesis
Recommended Citation
Alea, G. V. (1998). Novel tetrathiafulvalene derivatives and macrocycles with sugar units: Synthesis and characterization. Retrieved from https://animorepository.dlsu.edu.ph/etd_doctoral/1216
