The living anionic polymerization of isocyanates carried out using conventional initiators is associated with side reactions due to rapid initiation rates as well as back-biting by the growing chain, resulting in a lack of control on the molecular weight (MW) and molecular weight distribution (MWD) of the polymers. Successful control over the reaction was possible by using additives that could prevent back-biting. We find an initiator in sodium benzanilide (Na-BA), which has a slow initiation rate combined with additive function, so that use of an external additive is eliminated. The initiator has resulted in polymers with high yields and an unprecedented control over the MW and MWD. It is possible to introduce a number of functionalities at the termini of the polymer by using Na-BA derivatives as well as suitable terminating agents, leading to macromonomer, reactive and chiral polymers, and chiral macromonomer in approximately 100% yields. In the process, the finding has expanded the scope of polyisocyanates in diverse applications.
A well-defined amphiphilic coil-rod block copolymer, poly(2-vinyl pyridine)b-poly(n-hexyl isocyanate) (P2VP-b-PHIC), was synthesized with quantitative yields by anionic polymerization. A low reactive one-directional initiator, potassium diphenyl methane (DPM-K), was very effective in polymerizing 2-vinyl pyridine (2VP) without side reactions, leading to perfect control over molecular weight and molecular weight distribution over a broad range of initiator and monomer concentration. Copolymerization of 2VP with n-hexyl isocyanate (HIC) was carried out in the presence of sodium tetraphenyl borate (NaBPh 4 ) to prevent backbiting reactions during isocyanate polymerization. Terminating the living end with a suitable end-capping agent resulted in a P2VP-b-PHIC coil-rod block copolymer with controlled molecular weight and narrow molecular weight distribution. Cast film from a chloroform solution of P2VP-b-PHIC displayed microphase separation, characteristic of coil-rod block copolymers.
Introduction.Polyisocyanates are stiff polymers due to the amide bonds in the polymer main chain, and the polyisocyanate chains are twisted into helical conformations because of steric constraints. 1 Due to these structural properties, polyisocyanates have been studied in many applications such as chiral recognition materials, optical switches, and liquid crystal materials. 2 Since Shashoua and co-workers first reported the polymerization of isocyanates with sodium cyanide in dimethylformamide in 1959, 3 many researchers have studied the synthesis of polyisocyanates. 4 However, living polymerizations of isocyanates were difficult because of depolymerization by the formation of trimer. Despite this difficulty, Novak and co-workers synthesized poly-(n-hexyl isocyanate) using organotitanium initiators without trimer formation, even though it is a coordination polymerization. 5 Recently, Lee and co-workers succeeded in the synthesis of well-defined poly(3-(triethoxysilyl)propyl isocyanate)) using sodium naphthalene (Na-Naph) and 15-crown-5 (15C5) in THF at -98 °C under high vacuum. 6 The system successfully protected the backbiting of the anionic chain ends using a big countercation, the complex of Na-Naph-15C5. However, that is still unstable due to the greater distance between the active ends and the big ligand in polar solvent.In this study, poly(n-hexyl isocyanate) (PHIC) was synthesized via anionic polymerization as a function of reaction time at -98 °C in THF. We attempted to prevent the formation of trimers by utilizing sodium tetraphenylborate (NaBPh 4 ) as a common ion salt, which stabilizes the active anion by excess counter sodium cations. 7 A postpolymerization was carried out to confirm the living character of the active anionic chain ends of PHIC.Experimental Section. a. Materials. n-Hexyl isocyanate (HIC, Aldrich Chemical Co. Inc., 97%) was dried over CaH 2 for 24 h and distilled under reduced pressure. The resulting monomer was distilled once more from CaH 2 under vacuum. Tetrahydrofuran (THF, Fisher Scientific Co., GR grade) was distilled under N 2 after refluxing over Na for 4 h and stored as Na-Naph solution under vacuum at -30 °C.b. Anionic Polymerization. All polymerizations were carried out under high vacuum in a glass apparatus equipped with break-seals. In a typical polymerization procedure, the initiator solution, Na-Naph (0.10 mmol) in THF, was transferred into the reaction flask through the break-seal followed by 10-fold excess NaBPh 4 (0.97 mmol) in THF to the initiator. The
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.