A new thioether-bridged diimide-diacid (DIDA) monomer was synthesized from the condensation of 5,5 0 -thiobis(2-amino-4-methyl-thiazole) (DA) and trimellitic anhydride at 1 : 2 molar ratio. A series of novel organic-soluble poly(amide imide)s (PAIs) bearing flexible thioether linkages and heteroaromatic thiazole groups were synthesized from DIDA with various commercially available aromatic diamines (1-5) via a direct polycondensation method with triphenyl phosphite and pyridine. The resulting polymers were obtained in high yields and possessed inherent viscosities in the range of 0.47-0.91 dL g -1 . All of the polymers were amorphous in nature, showed good solubility and could be easily dissolved in amide-type polar aprotic solvents (e.g., N-methyl-2-pyrrolidone, dimethyl sulfoxide, and N,N-dimethylacetamide), and even dissolved in less polar solvents (e.g., pyridine and tetrahydrofuran). They showed excellent thermal stability with glass transition temperatures between 233-269 C and 10% weight loss temperatures in excess of 480 C in nitrogen and 450 C in air atmosphere. The flexible structure endowed the PAI films with good optical transparency. The optical transmittances of the PAI films at 450 nm were higher than 80% for the thickness of approximately 10 lm. Moreover, the thiazole moieties and flexible thioether linkages in the molecular chains of the PAIs provided them with high refractive indices of 1.7329-1.7509 and low birefringences of 0.0065-0.0098. V C 2012 Wiley Periodicals, Inc. J Appl Polym Sci 125: [1521][1522][1523][1524][1525][1526][1527][1528][1529] 2012