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1.
A. Levent Demirel Pınar Tatar Güner Bart Verbraeken Helmut Schlaad Ulrich S. Schubert Richard Hoogenboom 《Journal of Polymer Science.Polymer Physics》2016,54(7):721-729
Poly(2‐alkyl‐2‐oxazoline)s (PAOx) exhibit different crystallization behavior depending on the length of the alkyl side chain. PAOx having methyl, ethyl, or propyl side chains do not show any bulk crystallization. Crystallization in the heating cycle, that is, cold crystallization, is observed for PAOx with butyl and pentyl side chains. For PAOx with longer alkyl side chains crystallization occurs in the cooling cycle. The different crystallization behavior is attributed to the different polymer chain mobility in line with the glass transition temperature (Tg) dependency on alkyl side chain length. The decrease in chain mobility with decreasing alkyl side chain length hinders the relaxation of the polymer backbone to the thermodynamic equilibrium crystalline structure. Double melting behavior is observed for PButOx and PiPropOx which is explained by the melt‐recrystallization mechanism. Isothermal crystallization experiments of PButOx between 60 and 90 °C and PiPropOx between 90 and 150 °C show that PAOx can crystallize in bulk when enough time is given. The decrease of Tg and the corresponding increase in chain mobility at T > Tg with increasing alkyl side chain length can be attributed to an increasing distance between the polymer backbones and thus decreasing average strength of amide dipole interactions. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2016 , 54, 721–729 相似文献
2.
Chitoshi Kitamura Prof. Dr. Yasushi Abe Takuya Ohara Akio Yoneda Prof. Dr. Takeshi Kawase Prof. Dr. Takashi Kobayashi Dr. Hiroyoshi Naito Prof. Dr. Toshiki Komatsu Dr. 《Chemistry (Weinheim an der Bergstrasse, Germany)》2010,16(3):890-898
We synthesized a series of 1,4,7,10‐tetraalkyltetracenes using a new 2,6‐naphthodiyne precursor and 2,5‐dialkylfurans as starting materials (alkyl=methyl to hexyl). Surprisingly, the solid‐state color of the tetracenes ranges through yellow, orange, and red. Both yellow and red solids are obtained for the butyl derivative. Optical properties in solution show no marked differences; however, those in the solid state show characteristics that vary with alkyl side‐chain length: methyl, propyl, and pentyl derivatives are orange; ethyl and butyl derivatives are yellow; and another butyl and hexyl derivative are red. X‐ray analyses reveal that the molecular structures are planar, semi‐chair, or chair forms; the chair form takes a herringbone‐like arrangement and the other forms take slipped parallel arrangements. The mechanism of crystallochromy is discussed in terms of molecular structure, crystal packing, and calculations that take account of exciton coupling. 相似文献
3.
Atsushi Sudo Hiroshi Yamashita Takeshi Endo 《Journal of polymer science. Part A, Polymer chemistry》2011,49(16):3631-3636
p‐Toluenesulfonic acid (TsOH) and several alkyl p‐toluenesulfonates, that is, methyl p‐toluenesulfonate (TsOMe), cyclohexyl p‐toluenesulfonate (TsOCH), and neopentyl p‐toluenesulfonate (TsONP), were evaluated as initiators for the ring‐opening polymerization of benzoxazines. TsOH and TsOMe were highly efficient initiators that induced the polymerization at 60 and 80 °C, respectively. In contrast, TsOCH and TsONP did not initiate the polymerization below 100 °C, while they induced the polymerization at elevated temperatures, 120 and 150 °C, respectively. When TsOCH was used as an initiator, the corresponding polymerization rate was comparable to that observed for the polymerization with using TsOH as an initiator. These results suggested that neutral TsOCH and TsONP can be regarded as “thermally latent initiators,” which underwent the thermal dissociation at the elevated temperatures to generate the corresponding alkyl cations and/or TsOH as the initiators of the polymerization. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
4.
Richard Hoogenboom Hanneke M. L. Thijs Martin W. M. Fijten Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2007,45(23):5371-5379
The synthesis of statistical copolymers consisting of 2‐ethyl‐2‐oxazoline (EtOx) and 2‐“soy alkyl”‐2‐oxazoline (SoyOx) via a microwave‐assisted cationic ring‐opening polymerization procedure is described. The majority of the resulting copolymers revealed polydispersity indices below 1.30. The reactivity ratios (rEtOx 1.4 ± 0.3; rSoyOx = 1.7 ± 0.3) revealed a clustered monomer distribution throughout the polymer chains. The thermal and surface properties of the pEtOx‐stat‐SoyOx copolymers were analyzed before and after UV‐curing demonstrating the decreased chain mobility after cross‐linking. In addition, the cross‐linked materials showed shape‐persistent swelling upon absorption of water from the air, whereby as little as 5 mol % SoyOx was found to provide efficient cross‐linking. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 5371,–5379, 2007 相似文献
5.
Masatoshi Miyamoto Koji Tsutsui Yoshiharu Kimura 《Journal of polymer science. Part A, Polymer chemistry》1999,37(4):445-453
The isomerization polymerization of three alkyl glycidyl carbonates (4), i.e., glycidyl methyl carbonate (4a), ethyl glycidyl carbonate (4b), and glycidyl propyl carbonate (4c), catalyzed by methylaluminum bis(2,6‐di‐t‐butyl‐4‐methylphenoxide) (3) to afford novel poly(orthocarbonate)s, poly[(2‐alkoxy‐1,3‐dioxolane‐2,4‐diyl)oxymethylene]s (5a–c), is described. The polymerization proceeded best at around room temperature and gave 5 having several thousands of Mn. As the alkoxy chain of 4 was lengthened, the polymer yield decreased, while the polymer molecular weight increased. The yields of 5b and 5c, however, were improved by increasing the feed ratio of 3 to 4 from 0.04 to 0.10. The reactivity of 4 was discussed in relation to that of glycidyl alkanoates (1). © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 445–453, 1999 (See graphics.) 相似文献
6.
Imidazolium 2‐Substituted 4,5‐Dicyanoimidazolate Ionic Liquids: Synthesis,Crystal Structures and Structure–Thermal Property Relationships
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Dr. Suvendu Sekhar Mondal Holger Müller Dr. Matthias Junginger Alexandra Kelling Prof. Dr. Uwe Schilde Prof. Dr. Veronika Strehmel Prof. Dr. Hans‐Jürgen Holdt 《Chemistry (Weinheim an der Bergstrasse, Germany)》2014,20(26):8170-8181
Thirty six novel ionic liquids (ILs) with 1‐butyl‐3‐methylimidazolium and 3‐methyl‐1‐octylimidazolium cations paired with 2‐substitited 4,5‐dicyanoimidazolate anions (substituent at C2=chloro, bromo, methoxy, vinyl, amino, methyl, ethyl, propyl, isopropyl, butyl, pentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl and phenyl) have been synthesized and characterized by using differential scanning calorimetry (DSC), thermogravimetric analysis (TGA) and single‐crystal X‐ray crystallography. The effects of cation and anion type and structure on the thermal properties of the resulting ionic liquids, including several room temperature ionic liquids (RTILs) are examined and discussed. ILs exhibited large liquid and crystallization ranges and formed glasses on cooling with glass transition temperatures in the range of ?22 to ?68 °C. The effects of alkyl substituents of the imidazolate anion reflected the crystallization, melting points and thermal decomposition of the ILs. The Coulombic packing force, van der Waals forces and size of the anions can be considered for altering the thermal transitions. Three crystal structures of the ILs were determined and the effects of changes to the cations and anions on the packing of the structure were investigated. 相似文献
7.
A novel polymer‐dispersed liquid‐crystal film consisting of micrometer‐scale liquid‐crystal droplets in ultraviolet‐cured polymer composite matrices with cholesteric order was prepared and the influence of cure temperature on the phase separation was studied. The existence and pitch of the ethyl cyanoethyl cellulose cholesteric liquid‐crystalline phase were influenced by the existence of low molecular weight liquid crystals. The macromolecular cholesteric phase disappeared when the 4′‐n‐pentyl‐4‐cyano‐biphenyl concentration was over 40 wt %, and 4′‐n‐pentyl‐4‐cyano‐biphenyl domains were dispersed in the isotropic matrix of the polymer composite. © 2002 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 40: 1334–1341, 2002 相似文献
8.
Alkyl side chain length dependent compatibility of poly(4‐n‐alkylstyrene)s and 1,4‐rich polyisoprene blends
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Satoru Matsushima Atsushi Takano Yushu Matsushita 《Journal of Polymer Science.Polymer Physics》2017,55(23):1791-1797
We investigated the compatibility of blends of 1,4‐rich polyisoprene (1,4‐PI) and poly(4‐n‐alkylstyrene)s with six kinds of n‐alkyl side groups, that is, methyl, ethyl, propyl, butyl, hexyl, and octyl focusing on carbon number of alkyl groups. Poly(4‐methylstyrene)/1,4‐PI blend was turned out to be immiscible at all temperature range adopted in this work and poly(4‐ethylstyrene)/1,4‐PI blend revealed UCST type phase behavior, while the others were found to be compatible. The phase diagrams of poly(4‐ethylstyrene)/1,4‐PI blends were obtained by optical microscopy, and the temperature dependence of the Flory‐Huggins interaction parameter χ has been estimated to be χ = ?0.036 + 24/T by applying lattice theory, where T is the absolute temperature. From this relationship χ value at room temperature (298 K) was calculated to be 0.045, the value is reasonably low for miscible polymers system. © 2017 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2017 , 55 , 1791–1797 相似文献
9.
Meta M. Bloksma Sarah Rogers Ulrich S. Schubert Richard Hoogenboom 《Journal of polymer science. Part A, Polymer chemistry》2011,49(13):2790-2801
The synthesis and microwave‐assisted polymerization of a series of chiral 2‐oxazolines with varying alkyl pendant groups, namely R‐2‐ethyl‐4‐ethyl‐2‐oxazoline (R‐EtEtOx), R‐2‐butyl‐4‐ethyl‐2‐oxazoline (R‐BuEtOx), R‐2‐octyl‐4‐ethyl‐2‐oxazoline, 2‐nonyl‐4‐ethyl‐2‐oxazoline, and R‐2‐undecyl‐4‐ethyl‐2‐oxazoline (R‐UndeEtOx), are reported. A kinetic investigation of the polymerization of R‐EtEtOx revealed a living polymerization mechanism. The poly(2‐oxazoline)s containing an ethyl, butyl, and octyl pendant group form similar chiral structures according to circular dichroism measurements. When the pendant group is further elongated, the chiral structure becomes more flexible in trifluoroethanol and the thermal response in hexafluoroisopropanol (HFIP) significantly changes. The short‐range structure of poly‐R‐BuEtOx dissolved in HFIP is thermoresponsive in a complex way, due to HFIP hydrogen bonding to the polymeric amide groups, whereas the long‐range structure determined from small angle neutron scattering is insensitive to temperature demonstrating that only the local secondary structure changes with temperature. In addition, the chiral structure of poly‐R‐UndeEtOx depends on the polarity of the solvent. The short‐range structure becomes more flexible in polar solvents, most likely due to interactions with the amide groups disturbing the secondary structure. In contrast, the long‐range structural transition from an ellipsoid in the apolar n‐hexane to a rod structure in the polar n‐butanol is ascribed to better solvation of the long aliphatic side chains. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
10.
Reversible addition–fragmentation chain transfer polymerization of alkyl‐2‐cyanoacrylates: An assessment of livingness
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Cormac Duffy Marisa Phelan Per B. Zetterlund Fawaz Aldabbagh 《Journal of polymer science. Part A, Polymer chemistry》2017,55(8):1397-1408
Alkyl 2‐cyanoacrylates (CAs) are primarily used as instant adhesives, including those sold under the Loctite brand. The adhesive action can be inhibited with acid stabilizers allowing radical polymerization to be employed. The following article details the first attempted controlled/living radical polymerization of alkyl CAs: Reversible addition fragmentation chain transfer (RAFT) polymerization mediated by a poly(methyl methacrylate) dithiobenzoate macroRAFT agent for three different CA monomers (ethyl 2‐cyanoacrylate, n‐butyl 2‐cyanoacrylate, and 2‐phenylethyl cyanoacrylate) allowed the preparation of the first block copolymers of this challenging but commercially important monomer class. Nevertheless, GPC with UV detection indicated significant loss of the RAFT end‐group for all three CAs limiting control/living character. © 2016 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2017 , 55, 1397–1408 相似文献
11.
Synthesis of poly(2‐oxazoline)s with side chain methyl ester functionalities: Detailed understanding of living copolymerization behavior of methyl ester containing monomers with 2‐alkyl‐2‐oxazolines
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Maarten Vergaelen Bryn D. Monnery Saron Catak Jan C. M. van Hest Veronique Van Speybroeck Richard Hoogenboom 《Journal of polymer science. Part A, Polymer chemistry》2015,53(22):2649-2661
Poly(2‐oxazoline)s with methyl ester functionalized side chains are interesting as they can undergo a direct amidation reaction or can be hydrolyzed to the carboxylic acid, making them versatile functional polymers for conjugation. In this work, detailed studies on the homo‐ and copolymerization kinetics of two methyl ester functionalized 2‐oxazoline monomers with 2‐methyl‐2‐oxazoline, 2‐ethyl‐2‐oxazoline, and 2‐n‐propyl‐2‐oxazoline are reported. The homopolymerization of the methyl ester functionalized monomers is found to be faster compared to the alkyl monomers, while copolymerization unexpectedly reveals that the methyl ester containing monomers significantly accelerate the polymerization. A computational study confirms that methyl ester groups increase the electrophilicity of the living chain end, even if they are not directly attached to the terminal residue. Moreover, the electrophilicity of the living chain end is found to be more important than the nucleophilicity of the monomer in determining the rate of propagation. However, the monomer nucleophilicity can be correlated with the different rates of incorporation when two monomers compete for the same chain end, that is, in copolymerizations. © 2015 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2015 , 53, 2649–2661 相似文献
12.
F. Diaz Camacho R. Le Lagadec Alexander D. Ryabov L. Alexandrova 《Journal of polymer science. Part A, Polymer chemistry》2008,46(12):4193-4204
The cyclometalated complex [RuII(o‐C6H4‐py)(MeCN)4]PF6 ( 1 ) with a σ‐Ru? C bond and four substitutionally labile acetonitrile ligands mediates radical polymerization of different vinyl monomers, viz. n‐butyl acrylate, methyl methacrylate, and styrene, initiated by three alkyl bromides: ethyl 2‐bromoisobutyrate, methyl 2‐bromopropionate, and 1‐phenylethyl bromide. The polymerization requires the presence of Al(OiPr)3 and occurs uncontrollably as a conventional radical process. The variation of the molar ratio of the components of the reaction mixture, such as initiator, Al(OiPr)3 and catalyst, affected the polymerization rates and the molecular weights but did not improve the control. A certain level of control has been achieved by adding 0.5 eq of SnCl2 as a reducing agent. Tin(II) chloride decreased the rate of polymerization and simultaneously the molecular weights became conversion‐dependent and the polydispersities were also narrowed. Remarkably, the level of control was radically improved in the presence of excess of the poorly soluble catalyst ( 1 ), when the added amount of ( 1 ) was not soluble any more, i.e., under heterogeneous conditions, the system became adjustable and the living polymerization of all three monomers was finally achieved. Possible mechanisms of the ( 1 )‐catalyzed polymerization are discussed. © 2008 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 4193–4204, 2008 相似文献
13.
Costas N. Costa Costas S. Patrickios 《Journal of polymer science. Part A, Polymer chemistry》1999,37(11):1597-1607
α‐Hydroxy and α,ω‐dihydroxy polymers of 2‐(dimethylamino)ethyl methacrylate (DMAEMA) of various molecular weights were synthesized by group transfer polymerization (GTP) in tetrahydrofuran (THF), using 1‐methoxy‐1‐(trimethylsiloxy)‐2‐methyl propene (MTS) as the initiator and tetrabutylammonium bibenzoate (TBABB) as the catalyst. The hydroxyl groups were introduced by adding one 2‐(trimethylsiloxy) ethyl methacrylate (TMSEMA) unit at one or at both ends of the polymer chain. The ends were converted to 2‐hydroxyethyl methacrylate (HEMA) units after the polymerization by acid‐catalyzed hydrolysis. Gel permeation chromatography (GPC) in THF and proton nuclear magnetic resonance (1H‐NMR) spectroscopy in CDCl3 were used to determine the molecular weight and composition of the polymers. These mono‐ and difunctional methacrylate polymers can be covalently linked at the hydroxy termini to form star polymers and model networks, respectively. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1597–1607, 1999 相似文献
14.
Benoit Lessard Edwin Jee Yang Ling Marie Sylvianne Thérèse Morin Milan Marić 《Journal of polymer science. Part A, Polymer chemistry》2011,49(4):1033-1045
The controlled nitroxide‐mediated homopolymerization of 9‐(4‐vinylbenzyl)‐9H‐carbazole (VBK) and the copolymerization of methyl methacrylate (MMA) with varying amounts of VBK were accomplished by using 10 mol % {tert‐butyl[1‐(diethoxyphosphoryl)‐2,2‐dimethylpropyl]amino} nitroxide relative to 2‐({tert‐butyl[1‐(diethoxyphosphoryl)‐2,2‐dimethylpropyl]amino}oxy)‐2‐methylpropionic acid (BlocBuilder?) in dimethylformamide at temperatures from 80 to 125 °C. As little as 1 mol % of VBK in the feed was required to obtain a controlled copolymerization of an MMA/VBK mixture, resulting in a linear increase in molecular weight versus conversion with a narrow molecular weight distribution (Mw /Mn ≈ 1.3). Preferential incorporation of VBK into the copolymer was indicated by the MMA/VBK reactivity ratios determined: rVBK = 2.7 ± 1.5 and rMMA = 0.24 ± 0.14. The copolymers were found significantly “living” by performing subsequent chain extensions with a fresh batch of VBK and by 31P NMR spectroscopy analysis. VBK was found to be an effective controlling comonomer for NMP of MMA, and such low levels of VBK comonomer ensured transparency in the final copolymer. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献
15.
Greg Kaplan Greg Drake Kerri Tollison Leslie Hall Tommy Hawkins 《Journal of heterocyclic chemistry》2005,42(1):19-27
Quarternary salts based upon 3‐alkyl substituted 1‐amino‐1,2,3‐triazolium cations (alkyl = methyl, ethyl, nypropyl, 2‐propenyl, and n‐butyl) have been synthesized and characterized by vibrational spectra, multinuclear NMR, elemental analysis, and DSC studies. Subsequent diazotization of these salts results in the exclusive formation of 1‐alkyl‐1,2,3‐triazoles. Single crystal X‐ray studies were carried out for 1‐amino‐3‐methyl‐1,2,3‐triazolium iodide, 1‐amino‐3‐ethyl‐1,2,3‐triazolium bromide, 1‐amino‐3‐n‐propyl‐1,2,3‐triazolium bromide, and 1‐amino‐3‐n‐butyl‐1,2,3‐triazolium bromide as well as the starting heterocycle, 1‐amino‐1,2,3‐triazole, and all of the structures are discussed. 相似文献
16.
Olfa Glaied Christelle Delaite Guy Hurtrez Mathieu Joubert Philippe Dumas 《Journal of polymer science. Part A, Polymer chemistry》2005,43(11):2440-2447
Well‐defined macromonomers of poly(ethylene oxide) and poly(tert‐butyl methacrylate) were obtained by anionic polymerization induced directly by the carbanion issued from 2‐methyl‐2‐oxazoline. When ethylene oxide was added to this carbanion with lithium as the counterion, a new compound able to initiate the polymerization of ε‐caprolactone in an anionically coordinated way was synthesized, and this led to well‐defined poly(ε‐caprolactone) macromonomers. © 2005 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 43: 2440–2447, 2005 相似文献
17.
Richard Hoogenboom Hanneke M. L. Thijs Martin W. M. Fijten Bart M. van Lankvelt Ulrich S. Schubert 《Journal of polymer science. Part A, Polymer chemistry》2007,45(3):416-422
The microwave‐assisted statistical copolymerization of 2‐phenyl‐2‐oxazoline with 2‐methyl‐2‐oxazoline or 2‐ethyl‐2‐oxazoline is discussed in this contribution. Kinetic studies of these statistical copolymerizations as well as reactivity ratio determinations were performed to investigate the monomer distribution in these copoly(2‐oxazoline)s, demonstrating the formation of quasi‐diblock copolymers. In addition, the synthesis of copolymer series with monomer concentrations ranging from 0 to 100 mol % is described. These copolymer series were characterized with 1H NMR spectroscopy, gas chromatography, and gel permeation chromatography. Moreover, the glass‐transition temperatures and solubility of these copolymers were studied, and this revealing better mixing of poly(2‐methyl‐2‐oxazoline) (pMeOx) with poly(2‐phenyl‐2‐oxazoline) (pPhOx) than poly(2‐ethyl‐2‐oxazoline) (pEtOx) with poly(2‐phenyl‐2‐oxazoline) (pPhOx). © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 45: 416–422, 2007. 相似文献
18.
Uwe Beginn Gabriela Zipp Martin Mller 《Journal of polymer science. Part A, Polymer chemistry》2000,38(3):631-640
Crystallization and supramolecular aggregation of 3,4,5‐tris[(11‐methacryloyl‐undecyl‐1‐oxy)‐4‐benzyloxy]benzoate (1), 2‐methyl‐(1,4,7,10,13‐pentaoxabenzocyclopentadecane)‐3,4,5‐tris[(11‐methacryloyl‐undecyl‐1‐oxy)‐4‐benzoxyloxy]benzoate (2) and its 1 : 1 sodium triflate complex (2a) are described in solutions of methacrylate monomers. Formation of gels and subsequent polymerization yielded “supramolecular interpenetrating networks” consisting of an isotropic polymethacrylate resin, percolated by supramolecular aggregates of the solute, which are covalently connected to the resin phase. Compound 1 formed whisker‐type crystals, while 2 self‐organizes in networks of elongated supramolecular fibrils with diameters corresponding to the twofold length of one molecule. © 2000 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 38: 631–640, 2000 相似文献
19.
Prakash S. Sane Bhausaheb V. Tawade Indravadan Parmar Savita Kumari Samadhan Nagane Prakash P. Wadgaonkar 《Journal of polymer science. Part A, Polymer chemistry》2013,51(9):2091-2103
Two new initiators, namely, 4‐(4‐(2‐(4‐(allyloxy) phenyl)‐5‐hydroxypentane 2‐yl) phenoxy)benzaldehyde and 4‐(4‐(allyloxy) phenyl)‐4‐(4‐(4‐formylphenoxy) phenyl) pentyl 2‐bromo‐2‐methyl propanoate containing “clickable” hetero‐functionalities namely aldehyde and allyloxy were synthesized starting from commercially available 4,4′‐bis(4‐hydroxyphenyl) pentanoic acid. These initiators were utilized, respectively, for ring opening polymerization of ε‐caprolactone and atom transfer radical polymerization of methyl methacrylate. Well‐defined α‐aldehyde, α′‐allyloxy heterobifunctionalized poly(ε‐caprolactones) (Mn,GPC: 5900–29,000, PDI: 1.26–1.43) and poly(methyl methacrylate)s (Mn,GPC: 5300–28800, PDI: 1.19–1.25) were synthesized. The kinetic study of methyl methacrylate polymerization demonstrated controlled polymerization behavior. The presence of aldehyde and allyloxy functionality on polymers was confirmed by 1H NMR spectroscopy. Aldehyde‐aminooxy and thiol‐ene metal‐free double click strategy was used to demonstrate reactivity of functional groups on polymers. © 2013 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2013 相似文献
20.
Masatoshi Miyamoto Yasumichi Saeki Hidemasa Maeda Yoshiharu Kimura 《Journal of polymer science. Part A, Polymer chemistry》1999,37(4):435-444
The isomerization polymerizations of glycidyl propionate (1b), octanoate (1c), and stearate (1d) with methylaluminum bis(2,6‐di‐tert‐butyl‐4‐methylphenoxide) (3) were investigated. The polymerizations selectively gave poly(2‐alkyl‐1,3‐dioxolane‐4,2‐diyloxymethylene)s (2), although the polymer yield as well as the polymer molecular weight significantly decreased as the acyl chain of 1 was lengthened. These polymers readily hydrolyzed to glycerin and the corresponding fatty acids under mild conditions. The copolymerizations of glycidyl acetate (1a) with these monomers were also examined. In any combination, the composition of the obtained copolymer was essentially identical with the feed ratio, while both copolymer yield and molecular weight decreased as the feed of 1a was decreased. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 435–444, 1999 (See graphics.) 相似文献