Unsaturated alkoxy‐substituted poly(p‐phenylene 1,3,4‐oxadiazole)s: Synthesis and chemical–physical characterization

A new series of alkoxy‐substituted poly(p‐phenylene 1,3,4‐oxadiazole)s modified by the insertion of small percentages of various comonomers were synthesized through the precursor polyhydrazides. The comonomers used contained trans double bonds or meta‐alkoxy‐substituted aromatic rings to improve the solubility of the final polymers. The synthesized copolymers were chemically characterized by ¹H NMR and Fourier transform infrared spectroscopy. In some cases, the copolymers really showed improved solubility in organic solvents. The ¹⁵N solid‐state NMR technique was applied to examine the degree of conversion from the precursor polyhydrazides to the final polymers, which determined the effective conjugated length in the target polyoxadiazoles. Thermal stability and structural characteristics of all the polymers as well as a preliminary investigation on the optical properties of polyoxadiazoles are also reported. The copolymers retained high absorbance in the UV region and high transmission in the whole telecommunication range. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 3916–3928, 2003     

Synthesis and fluorescent properties of conjugated copolymers containing maleimide and fluorene units at the main chain

Yamamoto or Suzuki–Miyaura coupling polymerizations of 2,3‐diiodo‐N‐cyclohexylmaleimide with fluorene derivatives (2,7‐dibromo‐9,9′‐dihexylfluorene and 9,9′‐dihexylfluorene‐2,7‐diboronic acid) were carried out. The number‐average molecular weights (M_n) of the resulting copolymers were 2600–3500 by gel permeation chromatography analysis. The fluorescence emission of the alternating copolymer showed the emission maxima at 551 nm in THF. On the other hand, the random copolymers showed the bimodal emission peaks at 418–420 and 555–557 nm region, respectively. The fluorescence peaks of the random copolymers on the long wavelength region (555–557 nm) were attributed to the conjugated neighboring N‐cyclohexylmaleimide‐9,9′‐dihexylfluorene units in the polymer main chain. Furthermore, the copolymers exhibited the fluorescence solvatochromism by the difference of the polarity of solvents. The alternating and random copolymers showed the different fluorescence solvatochromism, and the emission colors are distinguishable by the naked eye, respectively. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4945–4956     

Synthesis and characterization of new alternating,amphiphilic, comblike copolymers of poly(ethylene oxide) macromonomer and N‐phenylmaleimide

A surface‐active p‐vinyl benzyloxy‐ω‐hydroxy‐poly(ethylene oxide) macromonomer containing 22 pendant structural units of ethylene oxide (St–PEO₂₂) was synthesized with an initiation method. Because of its solubility in a large variety of solvents, the free‐radical copolymerization with electron‐acceptor N‐phenylmaleimide (NPMI) was performed at 60 °C in benzene and tetrahydrofuran (THF) as isotropic media and in a water–THF mixture or water as a heterogeneous medium. Oil‐soluble 2,2′‐azobisisobutyronitrile and water‐soluble 4,4′‐azobis(4‐cyanovaleric acid) were used as the initiators at fixed concentrations. Two different St–PEO₂₂/NPMI comonomer ratios (1/1 and 3/7) at a fixed total comonomer concentration in the polymerization system were used. The structures, compositions, and microstructure peculiarities of the obtained alternating, amphiphilic, comblike copolymers were determined by NMR analysis. For the copolymers synthesized in hydrophilic media, differential scanning calorimetry showed, near the endothermic peak attributed to the melting of the poly(ethylene oxide) side chains, the presence of a second peak due to the partially ordered phase that could exist between the crystalline state and the isotropic melt. Also, the thermal stability of the obtained copolymers was studied with thermogravimetric analysis. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 479–492, 2005     

Characterization of poly(styrene‐co‐methacrylonitrile)s obtained by low‐temperature radiation polymerization and thermal degradation behavior measured by Py‐GC and CRTG

Poly(styrene‐co‐methacrylonitrile)s were polymerized in solutions with different polarities (n‐hexane and THF) by low‐temperature γ‐ray irradiation polymerization in a temperature range of −83.6–30 °C. It was found by IR measurement that the composition of the copolymers changed remarkably due to the effects of the polarity of solvents and the polymerization temperature. The thermal degradation behavior in the flash pyrolysis and in the continuous heating pyrolysis of these copolymers was measured by Py‐GC and controlled rate thermogravimetry (CRTG). The effects of the copolymer composition and sequence distribution on the thermal degradation behavior were investigated. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 3569–3577, 2000     

Cationic copolymerization of tetrahydrofuran with ethylene oxide in the presence of diols: Composition,microstructure, and properties of copolymers

Cationic copolymerization of tetrahydrofuran (THF) with ethylene oxide (EO) in the presence of diols leads to dihydroxy terminated telechelic copolymers. In the present article the influence of copolymerization conditions on the copolymer structure was studied in view of conclusions derived from studies of copolymerization kinetics and mechanism. It was shown that according to established copolymerization mechanism, the number average molecular weights increase linearly with conversion up to M_n ≅ 2500, hydroxyl end groups are bound exclusively to EO units and copolymers are composed of [EO]–[THF]_y segments. Microstructure of copolymers may be to some extent regulated by changing reaction conditions. Some physical properties of copolymers also were studied. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 3455–3463, 1999     

Grafting of poly(styrene‐co‐p‐chloromethyl styrene) with ethyl methacrylate via atom transfer radical polymerization catalyzed by CuCl/1,2‐dipiperidinoethane

Poly(styrene‐graft‐ethyl methacrylate) graft copolymer was prepared by atom transfer radical polymerization (ATRP) with poly(styrene‐co‐p‐chloromethyl styrene)s in various compositions as macroinitiator in the presence of CuCl/1,2‐dipiperidinoethane at 130 °C in N,N‐dimethylformamide. Both macroinitiators and graft copolymers were characterized by elemental analysis, IR, ¹H and ¹³C NMR, and differential scanning calorimetry. 1,2‐Dipiperidinoethane was an effective ligand of CuCl for ATRP in the graft copolymerization. The controlled growth of the side chain provided the graft copolymers with polydispersities of 1.60–2.05 in the case of poly(styrene‐co‐p‐chloromethyl styrene) (62:38) macroinitiator. Thermal stabilities of poly(styrene‐graft‐ethyl methacrylate) graft copolymers were investigated by thermogravimetric analysis as compared with those of the macroinitiators. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 668–673, 2003     

Synthesis of novel tetrahydrofuran‐epichlorohydrin [poly(THF‐b‐ECH)] macromonomeric peroxy initiators by cationic copolymerization and the quantum chemically investigation of initiation system effects

Cationic polymerization of tetrahydrofuran (THF) and epichlorohydrin (ECH) was performed with peroxy initiators synthesized from bis (4,4′‐bromomethyl benzoyl peroxide (BBP) or bromomethyl benzoyl t‐butyl peroxy ester (t‐BuBP) and AgSbF₆ or ZnCl₂ system at 0 °C to obtain the poly(THF‐b‐ECH) macromonomeric peroxy initiators. Kinetic studies were accomplished for poly(THF‐b‐ECH) initiators. Poly(THF‐b‐ECH‐b‐MMA) and poly(THF‐b‐ECH‐b‐S) block copolymers were synthesized by bulk polymerization of methyl methacrylate (MMA) and styrene (S) with poly(THF‐b‐ECH) initiators. The quantum chemical calculations for the block copolymers, the initiating systems of the cationic polymerization of THF and ECH were achieved using HYPERCHEM 7.5 program. The optimized geometries of the polymers were investigated with the quantum chemical calculations. Poly(THF‐b‐ECH) initiators having peroxygen groups were used for graft copolymerization of polybutadien (PBd) to obtain poly(THF‐b‐ECH‐g‐PBd) crosslinked graft copolymers. The graft copolymers were investigated by sol‐gel analysis. Swelling ratio values of the graft copolymers in CHCl₃ were calculated. The characterizations of the polymers were achieved by FTIR, ¹H NMR, GPC, SEM, TEM, and DSC techniques. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2896–2909, 2010     

Synthesis of periodic copolymers via ring‐opening copolymerizations of cyclic anhydrides with tetrahydrofuran using nonafluorobutanesulfonimide as an organic catalyst and subsequent transformation to aliphatic polyesters

To synthesize polyesters and periodic copolymers catalyzed by nonafluorobutanesulfonimide (Nf₂NH), we performed ring‐opening copolymerizations of cyclic anhydrides with tetrahydrofuran (THF) at 50–120 °C. At high temperature (100–120 °C), the cyclic anhydrides, such as succinic anhydride (SAn), glutaric anhydride (GAn), phthalic anhydride (PAn), maleic anhydride (MAn), and citraconic anhydride (CAn), copolymerized with THF via ring‐opening to produce polyesters (M_n = 0.8–6.8 × 10³, M_n/M_w = 2.03–3.51). Ether units were temporarily formed during this copolymerization and subsequently, the ether units were transformed into esters by chain transfer reaction, thus giving the corresponding polyester. On the other hand, at low temperature (25–50 °C), ring‐opening copolymerizations of the cyclic anhydrides with THF produced poly(ester‐ether) (M_n = 3.4–12.1 × 10³, M_w/M_n = 1.44–2.10). NMR and matrix‐assisted laser desorption/ionization time‐of‐flight mass spectra revealed that when toluene (4 M) was used as a solvent, GAn reacted with THF (unit ratio: 1:2) to produce periodic copolymers (M_n = 5.9 × 10³, M_w/M_n = 2.10). We have also performed model reactions to delineate the mechanism by which periodic copolymers containing both ester and ether units were transformed into polyesters by raising the reaction temperature to 120 °C. © 2012 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2012     

Synthesis,characterization, and self‐assembly of comb‐dendronized amphiphilic block copolymers

Novel amphiphilic comb‐dendronized diblock copolymers composed of hydrophobic Percec‐type dendronized polystyrene block and hydrophilic comb‐like poly(ethylene oxide) grafted polymethacrylate P(PEOMA) block were designed and synthesized via two steps of atom transfer radical polymerization (ATRP). The comb‐like P(PEOMA) prepared by ATRP of macromonomers (PEOMA) with two different molecular weights (M_n = 300 and 475) were used to initiate the sequent ATRP of dendritic styrene macromonomer (DS). The molecular weights and compositions of the obtained block copolymers were determined by ¹H NMR analysis. The copolymers with relatively narrow polydispersities (1.27–1.38) were thus obtained. The bulk properties of comb‐dendronized block copolymers were studied by using differential scanning calorimetry, polarized optical microscopy and wide‐angle X‐ray diffraction (WAXD). Similar to dendronized homopolymers, the block copolymers exhibited hexagonal columnar liquid‐crystalline phase structure. By using such amphiphilic comb‐dendronized block copolymers as building blocks, the rich self‐assembly morphologies, such as twisted string, vesicle, and large compound micelle (LCM), were obtained in a mixture of CH₃OH and THF. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4205–4217, 2008     

Fluorescence emission of amphiphilic copolymers bearing benzimidazole groups: Stimuli‐responsive behaviors in aqueous solution

A stimuli‐responsive amphiphilic copolymer poly(NIPAM_m‐b‐VBNBI_n), including N‐isopropylacrylamide (NIPAM) as a thermoresponsive unit and 1‐(4‐vinyl benzyl)‐2‐naphthyl‐benzimidazole (VBNBI) as a sensitive fluorophore unit, was designed and synthesized by reversible addition‐fragmentation chain transfer polymerization. The aqueous solutions of the copolymers exhibited reversible fluorescent response to pH and temperature. In addition, the copolymers showed aggregation‐induced fluorescence enhancement in THF/water mixture. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013, 51, 4459–4466     

Preparation of amphiphilic statistical copolymers of 2‐hydroxyethyl methacrylate with 2‐diethylaminoethyl methacrylate,precursors of water‐soluble copolymers

Statistical copolymers of 2‐hydroxyethyl methacrylate (HEMA) and 2‐diethylaminoethyl methacrylate (DEA) were synthesized at 50 °C by free‐radical copolymerization in bulk and in a 3 mol L^?1 N,N′‐dimethylformamide solution with 2,2′‐azobisisobutyronitrile as an initiator. The solvent effect on the apparent monomer reactivity ratios was attributed to the different aggregation states of HEMA monomer in the different solvents. The copolymers obtained were water‐insoluble at a neutral pH but soluble in an acidic medium when the molar fraction of the DEA content was higher than 0.5. The quaternization of DEA residues increased the hydrophilic character of the copolymers, and they became water‐soluble at a neutral pH when the HEMA content was lower than 0.25. © 2002 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 40: 2427–2434, 2002     

Synthesis and characterization of alternating copolymers containing triphenylamine as hole‐transporting units

A series of light‐emitting poly(p‐phenylene vinylene)s with triphenylamine units as hole‐transporting moieties in the main chain were synthesized via Wittig condensation in good yields. The newly formed vinylene double bonds possessed a trans configuration, which was confirmed by Fourier transform infrared and NMR spectroscopy. The high glass‐transition temperature (83–155 °C) and high decomposition temperature (>300 °C) suggested that the resulting copolymers possessed high thermal stability. These copolymers, especially TAAPV1, possessed a high weight‐average molecular weight (47,144) and a low polydispersity index (1.55). All the copolymers could be dissolved in common organic solvents, such as tetrahydrofuran (THF), CHCl₃, CH₂Cl₂, and toluene, and exhibited intense photoluminescence in THF (the emission maxima were located from 478 to 535 nm) and in film (from 478 to 578 nm). The low onsets of the oxidation potential (0.6–0.75 V) suggested that the alternating copolymers possessed a good hole‐transporting property due to the incorporation of triphenylamine moieties. © 2001 John Wiley & Sons, Inc. J Polym Sci Part A: Polym Chem 39: 3278–3286, 2001     

Energy migration in poly(N‐vinyl carbazole) and its copolymers with methyl methacrylate: Fluorescence polarization,quenching, and molecular dynamics

Fluorescence polarization and quenching measurements were used to examine intramolecular energy migration for poly(N‐vinyl carbazole) and copolymers of N‐vinyl carbazole with methyl methacrylate. Quenching measurements of the carbazole fluorescence by CCl₄ were performed in dilute solution in toluene, and fluorescence anisotropy, r, was measured for the chains dispersed in a solid matrix of poly(methyl methacrylate) (PMMA). The results suggested that the chains with a high carbazole content, that is, a high content of excimer trapping sites, do not show the highest values of the singlet energy‐migration rate. Isotropies, r^?1, of the samples in vitrified PMMA corroborated such conclusions. Molecular dynamics simulations on isotactic and syndiotactic trichromophoric copolymer fragments were used to obtain parameters related to the energy‐transfer process as a function of the methyl methacrylate content. The parameters from the simulations supported the interpretation of the experiments. © 2003 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 41: 1615–1626, 2003     

Photocurable and thermally stable polymers based on 1,4‐pentadien‐3‐one‐1‐p‐hydroxyphenyl‐5‐p‐phenyl methacrylate: Copolymerization with ethyl acrylate

1,4‐Pentadien‐3‐one‐1,5‐bis(p‐hydroxyphenyl) (PBHP) was prepared by reacting p‐hydroxybenzaldehyde and acetone in the presence of an acid catalyst. 1,4‐Pentadiene‐3‐one‐1‐p‐hydroxyphenyl‐5‐p‐phenyl methacrylate (PHPPMA) monomer was prepared by reacting PBHP dissolved in ethyl methyl ketone (EMK) with methacryloyl chloride in the presence of triethylamine. A free‐radical solution polymerization technique was used for synthesizing homo‐ and copolymers of different feed compositions of PHPPMA and ethyl acrylate (EA) in EMK as a solvent with benzoyl peroxide as a free‐radical initiator at 70 ± 1 °C. All the polymers were characterized with IR and ¹H NMR techniques. The compositions of the copolymers were determined with the ¹H NMR technique. The copolymer reactivity ratios were evolved with Kelen–Tudos (EA = 1.25 and PHPPMA = 0.09) and extended Kelen–Tudos (EA = 1.30 and PHPPMA = 0.09) methods. Q (0.48) and e (1.68) values for the new monomer (PHPPMA) were calculated with the Alfrey–Price method. UV absorption spectra for poly(PHPPMA) showed two absorption bands at 302 and 315 nm. The photocrosslinking properties of the polymer samples were examined with the solvent method. Thermal analyses of the polymers were performed with the thermogravimetric‐differential thermogravimetric technique. First, the decomposition temperatures started for poly(PHPPMA), copoly(EA‐PHPPMA) (62:38), and copoly(EA‐PHPPMA) (41:59) were at 350, 410, and 417 °C, respectively. A gel permeation chromatographic method was used for determining the polymer molecular weights (weight‐average molecular weight: 2.67 × 10⁴ and number‐average molecular weight: 1.41 × 10⁴) and polydispersity index (1.89). The solubility of the monomer and the copolymers occurred at 30 °C with solvents having different polarities. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 41: 1632–1640, 2003     

Synthesis and association of poly(N,N‐dimethylacrylamide) copolymers with perfluorocarbon pendent groups connected through polyethylene‐glycol tethers

The synthesis is reported of copolymers of N,N‐dimethylacrylamide (DMA) and methacrylates containing 2,2′‐dihydroperfluorodecanoyl (RF) groups separated from the methacrylate by long polyethylene glycol (PEG) tether groups (between 1000 and 14,000 Da). At concentrations of between 1 and 8 wt % the copolymers with macromonomer contents of 1 mol % or less give gels in organic solvents such as dioxane, THF, or methanol, as well as in water. Given the low molecular weights, this indicates very efficient association of very low numbers of RF groups. Association and gel formation is enormously enhanced in the presence of longer PEG tethers. This is consistent with smaller poly(N,N,‐dimethylacrylamide) (PDMA) intermolecular excluded volume effects that are mediated by the longer PEG tethers and possibly by the incompatibility of PEG and PDMA that may lead to the formation of PEG microdomains. This increases the local concentrations of the RF groups in the PEO domains that are not diluted by the PDMA chains, as would be the case in the absence of PEG tethers. © 2003 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 360–373, 2004     

Synthesis and properties of p-nitrophenylacetylene–phenylacetylene copolymers

Copolymers of phenylacetylene (PA) and p-nitrophenylacetylene (pNPA) with various monomers ratios were prepared and characterized. The solubility of copolymers is dependent on the number of PA units in the chain. They show a good degree of stereoregularity and the M_W s are in the 10³–10⁵ a.m.u. range, depending on the monomers and catalyst molar ratios. The soluble samples exhibit film-forming properties and the film-surface morphology may be varied by using different solvents. The copolymers give good electrical response to relative humidity variations. © 1998 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 36: 93–102, 1998     

Carbohydrate‐based amphiphilic diblock copolymers: Synthesis,characterization, and aqueous properties

Amphiphilic poly(ε‐caprolactone)‐b‐poly[(methacrylate‐graft‐poly(ethylene oxide))‐co‐6‐O‐methacryloyl‐D ‐galactopyranose] (PCL‐b‐P(MAPEO‐co‐GaMa)) with various compositions and molecular weights were synthesized via a controlled four‐step strategy. The first step involves the synthesis of functionalized poly(ε‐caprolactone) macroinitiator by ring‐opening polymerization (ROP) of ε‐caprolactone (CL) as initiated by aluminum triisopropoxide (Al(OⁱPr)₃). After selective bromination of the hydroxyl end‐group of the resulting α‐isopropoxy, ω‐hydroxy poly(ε‐caprolactone) by using 2‐bromoisobutyryl bromide, the controlled radical copolymerization of α‐methoxy, ω‐methacrylate poly(ethylene oxide) (MAPEO) with 6‐O‐methacryloyl‐1,2;3,4‐di‐O‐isopropylidene‐D ‐galactopyranose (DIGaMa) was performed by atom transfer radical polymerization (ATRP) in THF at 60 °C using CuBr ligated with 1,1,4,7,10,10 hexamethyltriethylenetetramine (HMTETA) as catalytic complex. In the final step, isopropylidene protective functions were selectively removed using an aqueous formic acid solution leading to the expected amphiphilic graft copolymers. The molecular characterization of those copolymers was performed by ¹H NMR spectroscopy and gel permeation chromatography (GPC) analysis. The self‐assembly of the copolymers into micellar aggregates as well as the related critical micellization concentration (CMC) in aqueous media were determined by dynamic light scattering (DLS) and fluorescence spectroscopy, respectively. In parallel, the morphology of the solid deposits of micellar aggregates was examined with atomic force microscopy (AFM). © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 3662–3672, 2008     

Donor–acceptor‐based poly(toluidine‐co‐chloroaniline)s: Synthesis and characterization

A series of poly(o‐/m‐toluidine‐co‐o‐/m‐chloroaniline) copolymers of different compositions were synthesized by an emulsion method with ammonium persulfate as the oxidant. The conductivity of the copolymers was two to five orders of magnitude higher than that of the homopolymers poly(o‐toluidine) and poly(m‐chloroaniline). Among the copolymers, the copolymer of o‐toluidine and m‐chloroaniline exhibited a maximum conductivity of 0.14 S cm^?1. The conductivity of these copolymers was also higher than that of poly(aniline‐co‐chloroaniline). The properties of the copolymers were greatly influenced by the positions of the substituents and the concentrations of the individual monomers in the feed. All the copolymers were completely soluble in polar solvents such as dimethyl sulfoxide and showed higher heat stability as the chloroaniline concentration increased. These effects could be interpreted in terms of extensive hydrogen bonding and interchain linking and, therefore, higher electron delocalization in these copolymers due to the presence of electron‐rich toluidine rings adjacent to electron‐deficient chloroaniline. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 1579–1587, 2005     

Statistical copolymers of norbornene and 5‐vinyl‐2‐norbornene by a ditungsten complex mediated ring‐opening metathesis Polymerization: Synthesis,thermal properties,and kinetics of thermal decomposition

Statistical copolymers of norbornene (NBE) with 5‐vinyl‐2‐norbornene (VNBE) were prepared by ring‐opening metathesis polymerization, employing the triply bonded ditungsten complex Na[W₂(μ‐Cl)₃Cl₄(THF)₂].(THF)₃. NMR measurements revealed that the side vinyl groups of the VNBE monomer remain intact during the copolymerization reaction. The reactivity ratios were estimated using the Finemann–Ross (FR), the inverted FR, and the Kelen–Tüdos graphical methods. Structural parameters of the copolymers were obtained by calculating the dyad sequence fractions, which were derived using the monomer reactivity ratios. The glass transition temperatures, T_g, of the copolymers were measured by differential scanning calorimetry measurements and were examined in the frame of several theoretical equations allowing the prediction of these T_g values. The best fit was obtained using methods that take into account the monomer sequence distribution of the copolymers. Finally, the kinetics of the thermal decomposition of the copolymers was studied by thermogravimetric analysis in the frame of the Ozawa–Flynn–Wall and Kissinger methods. © 2013 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2013 , 51, 4835–4844     

Helix‐sense‐selective copolymerization of triphenylmethyl methacrylate with chiral 2‐isopropenyl‐4‐phenyl‐2‐oxazoline

The asymmetric induction leading to a one‐handed helix was investigated in the anionic and radical copolymerization of triphenylmethyl methacrylate (TrMA) and (S)‐2‐isopropenyl‐4‐phenyl‐2‐oxazoline ((S)‐IPO), and highly isotactic copolymers with a reasonable optical activity were obtained. In the anionic copolymerization, the optical activity of the obtained copolymers depended on the polarity of solvents, and a highly optically active copolymer was produced in the copolymerization in toluene. The chiral oxazoline monomer functioned not only as a comonomer but also as a chiral ligand to endow the polymer with large negative optical rotation in the copolymerization with TrMA. The copolymers with small positive optical rotation were obtained in THF, indicating that IPO unit may work only as the chiral monomer that dictates the helical sense via copolymerization with TrMA. The isotacticity of the obtained copolymers depended on the contents of TrMA units in the copolymers, but was almost independent of the solvent for copolymerization. In the radical copolymerization, the obtained copolymers exhibited small optical activities. It seemed that the chiral monomer cannot induce one‐handed helical structure of TrMA sequences even if the sequences probably have a high isotacticity. © 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019 , 57, 441–447