Polyester synthesis from the alternating copolymerization of epoxides with cyclic anhydrides via a metal-free route remains a key challenge. This work reports the development of a highly active organocatalytic route for the copolymerization of a spectrum of epoxides and cyclic anhydrides. Fully alternating polyesters were synthesized by a variety of organic Lewis acid–base pairs including organoboranes and quaternary onium salts. The effect of the acidity, type, and size of Lewis pairs on the catalytic activity and selectivity of the copolymerization is presented. The undesirable transesterification and etherification were effectively suppressed even in the case of complete conversion of the cyclic anhydride. This could be ascribed to the formation of a unique tetracoordinate bond-carboxylate (or alkoxide) anion. The Lewis pairs are highly active, with a turnover frequency of 102 and 303 h–1 for the copolymerization of propylene oxide with maleic anhydride and phthalic anhydride, respectively, at 80 °C. Block polyester with narrow polydispersity of 1.05 was achieved via a sequential addition strategy. This work provides robust organocatalysts for the selective copolymerization of epoxides with cyclic anhydrides.
Scheme1.Chain transfer reaction (M + represents the organic or inorganic counterion).Scheme2.Masking anion strategy for fast, living, and regioselective ROP of PO [P2:1-tert-butyl-2,2,4,4,4-pentakis(dimethylamino)-2l 5 ,4l 5 -catenadi (phosphazene); P1: tert-butylimino tris(dimethylamino)phosphorene; DBU:1,4,0]undec-7-ene; MTBD: N-methyl-1,5,7-triazabicyclododecene].
It is a challenging topic to disconnect a linear polymer selectively at the mechanophore site by an external force in a "cold" fashion. In this work, the effect of the power output of ultrasonication on the selective cleavage at the centered urfuryl-maleimide Diels−Alder (DA) mechanophore of poly(methyl acrylate)s (DA-PMA-a and DA-PMA-b) were quantitatively investigated by comparative study on experimental and simulated chain scission kinetics as well as high-resolution 1 H NMR spectroscopy (600 MHz). At low power output of the ultrasonication (2.10 W), DA-PMA-a with M n of ca. 2M lim (M lim , below which no further chain scission was observed) presented a DI (degradation index)−t (sonication time) plot with a turnover point at ca. 1.0 and no clear variation of the molecular weight after the turnover, which met well with the calculated center cleavage mode. At 5.52 W, DA-PMA-a and a poly(methyl acrylate) that contained two centered ester bonds (ester-PMA) presented similar DI−t plots with turnover points less than 1.0 within same sonication times, while poly(methyl acrylate) with fully carbon−carbon chain (PMA) had a turnover at DI value of ca. 0.5. By way of contrast, high power output of the ultrasonication (5.52 W) caused a possible cleavage of ester bonds of DA-PMA-a, which would mask the selective cleavage at the DA site. High-resolution 1 H NMR result of DA-PMA-b (115.8 kDa, M n was slightly higher than 2M lim ) showed that DA conversions were up to 55% under 2.10 W and 38% under 5.52 W. The kinetics from GPC traces and 1 H NMR results of DA-PMA-b as well as 1 H NMR results of DA-PMA-c (68.4 kDa, M n was slightly higher than M lim ) under sonication confirmed the observation that low power output favored selective chain scission at DA site. The turnover point in the DI−t plot might be used as characteristic parameter to gauge the selective chain scission at mechanophore site for single mechanophore-centered polymers.
Adding metals in synthetic polymers is of broad interest to design multifunctional materials, particularly harnessing unique properties and functionalities not found in pure organic polymers. Other than simple emergence of...
We studied the aggregation-induced emission (AIE) phenomenon in a nanoconfined environment, where the AIE-active molecule, namely, 1,1,2,2-tetrakis(4-methanoylphenyl)ethane (TPE-4ALD), was held in space via four acylhydrazone bonds within the thermosensitive microgel networks. The thermosensitive microgels, namely N-AH-TPE, were synthesized via the copolymerization of N-isopropylacrylamide (NIPAM) and 4-acylhydrazine-(2-hydroxy-3-(methacryloxypropyl)pyridine hydrochloride (AH monomer) with TPE-4ALD as cross-linker via surfactant free emulsion polymerization (SFEP) in aqueous solution at 70 °C. Acylhydrazone-bonded tetraphenylethene (TPE-4AH) moieties were thus constructed and worked as the fluorophore in N-AH-TPE microgels. The aqueous suspensions of N-AH-TPE microgels exhibit strongly bluish-green fluorescence under ultraviolet excitation because the four arms of TPE-4AH moieties were held and their intramolecular motions are strongly restricted. It is estimated that there is one TPE-4AH moiety per about 394 nm 3 for the swollen N-AH-TPE microgels. The fluorescent properties of N-AH-TPE microgels can be modulated via the change of hydrophilic and hydrophobic environments of TPE-4AH moieties exerted by external stimuli, like addition of various good solvents for TPE-based structures, i.e., N,N-dimethylformamide (DMF), methanol, ethanol, tetrahydrofuran (THF), and N,Ndimethyl sulfoxide (DMSO), varying the solution temperature as well as the counteranions of the microgels. An unusual enhancement in the fluorescent intensity is observed when specific amounts of organic solvent are added into the aqueous suspensions of N-AH-TPE microgels, which can be attributed to the cononsolvency of the polyNIPAM network chains. The shrinkage of N-AH-TPE microgels caused by the cononsolvency effect further strengthens the confinement of TPE-4AH moieties and hence enhances the fluorescent emission of the microgels even though the organic solvents added are good solvents for TPE-4AH. Increasing the solution temperature of N-AH-TPE microgels or introducing hydrophobic counteranions into the microgels also significantly enhances the fluorescent emission of the microgels.
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