IN 2001, SHARPLESS AND HIS CO-WORKERS SUCCESSFULLY OPTIMIZED THE REACTION OF AZIDE AND TERMINAL ALKYNE LEADING TO 1, 2, 3-TRIAZOLE VIA COPPER (I) CATALYSIS, SUBSEQUENTLY NAMED AS ONE OF ‘‘click’’ chemistry. THIS CONCEPT OF POPULAR REACTION HAS DRAWN WIDESPREAD ATTENTION DUE TO ITS HIGH EFFICIENCY, QUANTITATIVE YIELDS AND SELECTIVITY UNDER MILD REACTION CONDITIONS. THESE ADVANTAGES HAVE BEEN PARTICULARLY USEFUL IN THE AREA OF POLYMER chemistry. POLYMERS WITH DIFFERENT TOPOLOGIC STRUCTURES, INCLUDING LINEAR, BLOCK, STAR POLYMERS AND DENDRIMERS, HAVE BEEN REPORTED. THIS TECHNIQUE HAS ALSO BEEN WIDELY USED IN MATERIALS SCIENCE, SUCH AS BIOCONJUGATES AND VERSATILE FUNCTIONAL POLYMERS. IN VERY RECENT YEARS, click REACTIONS HAVE ALSO BEEN USED FOR THE SYNTHESIS OF LINEAR MAIN-CHAIN POLYTRIAZOLES BY THE STEP-GROWTH POLYMERIZATION. IN THIS INVESTIGATION, OUR AIM IS TO UTILIZE THE click REACTION TO SYNTHESIZE POLYMERS CONTAINING OXADIAZOL AND TRIAZOL RINGS IN THEIR BACKBONES FROM MONOMERS HAVING DIAZIDE AND DIALKYNE END GROUPS (SCHEME 1).