Transparent Aromatic Polyimides Derived from Thiophenyl-Substituted Benzidines with High Refractive Index and Small Birefringence

• Published in: Macromolecules 2015-06, Vol.48 (11), p.3462-3474
• Main Authors: Tapaswi, Pradip Kumar, Choi, Myeon-Cheon, Jeong, Keuk-Min, Ando, Shinji, Ha, Chang-Sik
• Format: Article
• Language: English
• ISSN: 0024-9297; 1520-5835
• DOI: 10.1021/acs.macromol.5b00432

2,2′-Bis­(thiophenyl)­benzidine (BTPB) and 2,2′-bis­(4-chlorothiophenyl)­benzidine (BCTPB) were synthesized via a benzidine rearrangement reaction of the corresponding hydrazobenzene derivatives obtained after the reduction of (3-nitrophenyl)­(phenyl)­sulfane and (4-chlorophenyl)­(3-nitrophenyl)­sulfane, respectively. Transparent polyimides (PIs) with high refractive indices and small birefringences as well as good thermomechanical stabilities were synthesized by the conventional two-step thermal polycondensation of BTPB and BCTPB with five different dianhydrides in N-methyl-2-pyrrolidone. 3,3′,4,4′-Biphenyltetracarboxylic dianhydride (BPDA)/BCTPB PI, a fully aromatic and non-fluorinated PI, with a highly distorted noncoplanar conformation of the main chain was transparent and colorless with a transmittance of ∼83% and >88% at 450 nm and in the visible region, respectively. In addition, all six non-fluorinated sulfur-containing aromatic PIs exhibited high average refractive indices (1.7112–1.7339), and small birefringences (0.0007–0.0022) at 633 nm, because of the high atomic polarizability of sulfur and the rigid bulky molecular structure of BTPB and BCTPB. The more effective steric effect caused by bulky 4-chlorothiophenyl in BCTPB improved the optical transparency but decreased the average refractive indices of BCTPB-based PIs compared to BTPB-based PIs.