Weilin Sun

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Name: sun weilin; 孙维林
Organization: Zhejiang university
Department: Key Laboratory of Macromolecular Synthesis and Functionalization, Department of Polymer Science and Engineering
Title: Professor

TOPICS

Co-reporter:Yan-hua Wang;Dong Xiang;Rong Ren;Jin Luo
Chinese Journal of Polymer Science 2014 Volume 32( Issue 11) pp:1500-1506
Publication Date(Web):2014 November
DOI:10.1007/s10118-014-1532-8
L-lactide (LLA) homopolymerization and copolymerization with ɛ-caprolactone (CL) in toluene initiated by tetrahydrosalen-supported yttrium borohydride complex were systematically investigated. A possible mechanism of LLA homopolymerization was proposed according to the 1H-NMR result. In addition, PCL-b-PLLA copolymers were synthesized by sequential addition of monomers and their structure was characterized by GPC, 1H-NMR and 13C-NMR.
Co-reporter:Lianbin Wu;Qiu Chen;Zhiqing Lv
Journal of Sol-Gel Science and Technology 2011 Volume 60( Issue 2) pp:
Publication Date(Web):2011 November
DOI:10.1007/s10971-011-2581-x
A novel alkoxysilylated derivative based on 2,2′-diamino-4,4′-bithiazole (DABTH) was firstly synthesized. The corresponding polysilsesquioxane (PBSIBTH) and its metal complexes (PBSIBTH-Eu3+, PBSIBTH-Tb3+ and PBSIBTH-Ni2+) were also obtained via sol–gel method, respectively. The morphology of their xerogels was investigated by scanning electron microscopy means. The magnetic measurements of these polymer complexes show all obtained solid materials feature soft ferromagnet properties at low temperature. The metal ions in polymer complexes have a significant influence on both microstructure and magnetic properties.
Co-reporter:Dong Xiang;Jian-fang Yu;Wei-lin Sun 孙维林
Chinese Journal of Polymer Science 2011 Volume 29( Issue 3) pp:296-299
Publication Date(Web):2011 May
DOI:10.1007/s10118-011-1041-y
The biphenol based discrete ion-pair rare earth complexes, [Ln(EDBP)2(DME)Na(DME)3] [Ln = Er(1), Yb(2), Sm(3)], were prepared and used as catalysts for the ring-opening polymerization (ROP) of 2,2-dimethyltrimethylene carbonate (DTC). Three complexes show moderate activities for the polymerization, and the catalytic activities increase in the following sequence: (Yb < Er < Sm). The effect of different ratios of [DTC]/[Ln], polymerization temperature and time on the polymerization was investigated. Moreover, PDTC without ether unit developed from possible CO2 elimination was prepared.
Co-reporter:Jing Huang;Jian-fang Yu;Han-jian Yu
Chinese Journal of Polymer Science 2011 Volume 29( Issue 3) pp:390-396
Publication Date(Web):2011 May
DOI:10.1007/s10118-011-1044-8
The poly(2,2-dimethyltrimethylene carbonate) (PDTC) with one hydroxyl and one formate terminal functions was synthesized by in situ generated, tetrahydrosalen stabilized yttrium borohydride complex. The influences of monomer/initiator molar ratio, temperature and reaction time on polymerization of DTC were investigated. Under the condition: [DTC]/[I] = 500, 55°C, toluene: 0.5 mL, DTC: 0.6 g, PDTC with Mn = 15600 and PDI = 2.15 was obtained. Through 1H-NMR and 13C-NMR analyses, the structure of PDTC was characterized and a coordination-insertion mechanism was proposed. In addition, the random copolymerization of DTC and caprolactone (CL) initiated by rare-earth borohydride compound was studied. The microstructure of PDTC-co-PCL includes four diads: DTC-CL, CL-CL, DTC-DTC and CLDTC, which were determined by the specific signals in 1H-NMR spectra. Based on the typical signals of the formate (δ=8.08) and hydroxyl (δ = 3.34) end groups of PDTC-co-PCL, a mechanism involving DTC monomer inserts before CL during the initiation process was presumed. Furthermore, the thermal properties of amorphous copolymer were characterized by differential scanning calorimetry (DSC). The results support the random structure of PDTC-co-PCL.
Co-reporter:Weihong Lin, Weilin Sun, Jun Yang, Qihang Sun and Zhiquan Shen
The Journal of Physical Chemistry C 2009 Volume 113(Issue 39) pp:16884-16895
Publication Date(Web):September 9, 2009
DOI:10.1021/jp900508p
The novel copolymer poly(5-methacryloylamido-1,10-phenanthroline-co-methacrylic acid) (PMPMA) containing a phenanthroline ring was prepared by free radical polymerization. The synthesized monomer and copolymer have been confirmed by FT-IR, 1H NMR spectra, and element analysis. A series of multilayer films, which were fabricated via layer-by-layer self-assembly with the polymer PMPMA and the transition metal neutralized poly(styrene 4-sulfonate) (PSSNi or PSSCu) on thin plastic substrate polyethylene film (PE), were described. The coordination interaction between the two nitrogen atoms of the PMPMA and the transition metal ions of the PSSM was the driving force for building up the multilayer film, which was identified by infrared spectroscopy. UV−vis spectra and AFM images were applied to monitor these films, and the results indicate that the assembling process is relatively uniform. The magnetic behavior was examined as a function of magnetic field strength at 5 K and as a function of temperature (5−300 K). It is found that the films exhibit different magnetic properties from diamagnetic to magnetic transition to strongly ferromagnetic with the increasing cycles of film deposition. The magnetic results show that the different number of assembling layers can infect the alignment of adjacent paramagnetic spins from short linear to tridimensional fashion and induce different magnetic phenomena. The present study will provide a new mechanism to prepare organic materials with different demands for magnetic property.
Co-reporter:Weihong Lin, Weilin Sun, Jun Yang and Zhiquan Shen
The Journal of Physical Chemistry C 2008 Volume 112(Issue 46) pp:18217-18223
Publication Date(Web):2017-2-22
DOI:10.1021/jp806196s
The preparation and magnetism of four multilayer films, (DABT/Ni2+/PAA)15×2, (DABT/Cu2+/PAA)15×2, (PAA/DABT)20×2−Ni2+, and (PAA/DABT)20×2−Cu2+, which were obtained by self-assembly of 2,2′-diamino-4,4′-bithiazole (DABT), poly(acrylic acid) (PAA), and transition metal ions (Cu2+ or Ni2+) on polyethylene (PE) substrate, were described. The driving force for building up the multilayer film was identified by infrared spectroscopy. UV−vis spectra and AFM images were applied to characterize these films and indicate the uniform assembling process. The magnetic behavior was examined as a function of magnetic field strength at 4 K and as a function of temperature (4−300 K). All films display good soft ferromagnetic properties, even affected by the diamagnetic substrate. It is found that (PAA/DABT)20×2−Ni2+ exhibits a fairly high value of relative saturation magnetization (Ms = 37.3 emu/g), while (DABT/Ni2+/PAA)15×2 exhibits a high Curie−Weiss temperature (θ = 242 K). The magnetic results show that different assembling processes can infect the alignment of adjacent paramagnetic spins and induce different magnetic phenomena.
Co-reporter:Zhiquan Shen;Weihong Lin
Polymers for Advanced Technologies 2007 Volume 18(Issue 12) pp:959-962
Publication Date(Web):22 NOV 2007
DOI:10.1002/pat.882

A novel linear polymer (PFABT) containing bithiazole rings was synthesized by polycondensation of 2,2′-diamino-4,4′-bithiazole (DABT) and formaldehyde. The complexes of PFABT with two transition metal ions (Fe2+, Cu2+) were prepared for the first time. The polymer was determined through FT-IR, 1H-NMR and elemental analysis (EA), and the complexes were characterized by FT-IR. The magnetic behaviors of these complexes were measured as a function of magnetic field strength (0–50 kOe) at 4 K and as a function of temperature (4–300 K) under an applied magnetic field of 30 kOe. The results show that PFABT-Cu2+ is a ferromagnet while PFABT-Fe2+ is an anti-ferromagnet. Copyright © 2007 John Wiley & Sons, Ltd.

Co-reporter:Weilin Sun;Zhiquan Shen;Ping Zheng
Journal of Applied Polymer Science 2006 Volume 100(Issue 2) pp:1289-1293
Publication Date(Web):30 JAN 2006
DOI:10.1002/app.23520

N-2-Thiazolylmethacrylamide (NTMA) was polymerized by a radical route to obtain the polymer in good yields. The complexes of PolyNTMA with three rare earth ions Nd(III), Pr(III), and Sm(III) were prepared for the first time. FTIR and 1H NMR were applied to characterize these materials. The magnetic behavior of PolyNTMA–metal complexes was examined as a function of applied magnetic field at 4 K and as a function of temperature (4–300 K) at an applied magnetic field of 30 kOe. It was found that Pr(III) complex exhibits an antiferromagnetic property, while Nd(III) and Sm(III) complexes exhibit a special magnetic property different from the typical magnet. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1289–1293, 2006

Co-reporter:Jun Yang;Zhuxian Zhou;Zhiquan Shen
Journal of Applied Polymer Science 2006 Volume 101(Issue 1) pp:443-446
Publication Date(Web):25 APR 2006
DOI:10.1002/app.23266

A novel polymer (poly[2,2'-(4,4'-bithiazolylene)][N-(2-ethylhexyl)-3,6-carbazylene] (PBTCA) was first synthesized from 2,2′-diamino-4,4′-bithiazole and N-(2-ethylhexyl)-3,6-diformylcarbazole. The structure of the polymer was determined with IR and 1H-NMR spectroscopy. The PBTCA–Nd3+ complex was prepared via the mixing of neodymium trichloride hexahydrate and PBTCA in dimethyl sulfoxide under a nitrogen atmosphere. The magnetic behaviors of the Nd3+ complex of a poly(Schiff base) were measured as a function of the magnetic field strength (0–50 kOe) at 4 K and as a function of the temperature (4–300 K). The results show that PBTCA–Nd3+ is a ferromagnet when the temperature is below 15 K, and above that, it is a diamagnet. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 101: 443–446, 2006

Co-reporter:Ping Zheng;Liming Jiang;Zhiquan Shen
Journal of Applied Polymer Science 2005 Volume 98(Issue 1) pp:83-87
Publication Date(Web):8 JUL 2005
DOI:10.1002/app.22031

N-2-thiazolyl(meth)acrylamides were polymerized by a radical route to obtain polymers in good yields. The polymers, with a pendent heterocyclic group, are soluble in common organic solvents, which allow the corresponding metal complexes with higher loads to be prepared easily. FTIR, 1H NMR, and energy-dispersive X-Ray spectroscopy (EDX) were applied to characterize these materials. The magnetic behavior of poly(N-2-thiazolyl(meth)acrylamide)-Fe(II) complexes was examined as a function of applied magnetic field at 4 K and as a function of temperature (4 ∼ 300 K) at an applied magnetic field of 1 ∼ 3 kOe, exhibiting the characteristics of a ferromagnet. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 98: 83–87, 2005

Co-reporter:Yanbing Lu;Zhiquan Shen
Journal of Applied Polymer Science 2005 Volume 96(Issue 4) pp:979-982
Publication Date(Web):1 MAR 2005
DOI:10.1002/app.20865

The polymerization of N-phenylmaleimide was carried out with the binary rare-earth coordination catalyst lanthanum phosphonate [La(P507)]–trisobutyl aluminum [Al(i-Bu)3] in toluene at 60°C. The dependence of the polymerization on the polymerization time, the molar ratio of Al(i-Bu)3 to La(P507), and the concentration of the catalyst were studied. The structures of the resultant polymer were characterized with 1H-NMR, 13C-NMR, and Fourier transform infrared spectrophotometry, and the thermal properties of the polymer were measured with thermogravimetric analysis. © 2005 Wiley Periodicals, Inc. J Appl Polym Sci 96: 979–982, 2005

Co-reporter:Weilin Sun;Liming Jiang
Polymers for Advanced Technologies 2005 Volume 16(Issue 8) pp:646-649
Publication Date(Web):13 JUN 2005
DOI:10.1002/pat.622

A novel polymer resulting from the polycondensation of 2,2′-diamino-4,4′-bithiazole (DABT) with 5,5′-methylene-bis-salicylaldehyde (MBSA) and its ferric complex are described. Analyses of Fourier transform infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS) revealed that both bithiazole residue and Schiff-base moiety acted as coordination sites for Fe3+ ions in the polymeric matrix. The magnetic behavior of the complex was studied as a function of magnetic field strength (0–60 kOe) at 25 K and as a function of temperature (5–300 K) at a magnetic field strength of 30 kOe. The hysteretic loop was measured at 5 K for the complex showing coercivity (Hc) of 20 Oe and remnant magnetization (Mr) of 0.002 emu/g, which is much lower than those of bithiazole-based polymeric complexes previously reported. The results indicated that the present complex is of the typical characteristics of a soft ferromagnet. Copyright © 2005 John Wiley & Sons, Ltd.

Co-reporter:Jiang Li-Ming;Sun Wei-Lin;Shen Zhi-Quan
Chinese Journal of Chemistry 2005 Volume 23(Issue 6) pp:
Publication Date(Web):12 JUL 2005
DOI:10.1002/cjoc.200590791

A new kind of π-conjugated heterocyclic poly(Schiff base) was firstly prepared by the condensation reaction between tetrathiatetrahydropentalene-type diketone and bithiazole-diamine in good yields. The polymers were characterized by VPO, FTIR and 1H NMR spectroscopy. A large bathochromic shift was observed in UV-Vis spectra for these polymers due to the π-π* transition in the conjugated main chain. Brief examination indicated that the nitrogen- and sulfur-containing polymers exhibited an excellent chelating tendency to metal ions and the corresponding polymeric complexes would be expected to have potential in applications.

Co-reporter:Bingjing He, Weilin Sun, Miao Wang, Shuang Liu, Zhiquan Shen
Materials Chemistry and Physics 2004 Volume 84(Issue 1) pp:140-145
Publication Date(Web):March 2004
DOI:10.1016/j.matchemphys.2003.11.018
A new way was used to chemically synthesize a series of novel complexes of heteroaromatic polymer-connected SWNTs and metal ions (Fe2+, Nd3+). These derivations of SWNTs were characterized by Fourier transform infrared instrument (FTIR), elemental analysis (EA), the transmission electron microscopy (TEM), thermogravimetric analysis (TGA) and Raman spectrum, and better regularity is shown. Moreover, the magnetic behavior of these polymeric complexes was measured as a function of temperature (0–300 K) and as a function of magnetic field strength (0–40 kOe) at 5 K. The results of measurements indicate these complexes have special soft-ferromagnetic properties.
Co-reporter:Caiping Lin;Liming Jiang;Liqun Wang;Zhiquan Shen
Journal of Applied Polymer Science 2004 Volume 93(Issue 3) pp:1264-1270
Publication Date(Web):4 MAY 2004
DOI:10.1002/app.20581

Two novel bithiazole-containing polyamides, DClAI and DTTPA, and their complexes were synthesized by condensation and complexation. Novel homogeneous composite films were prepared by in situ blending these complexes with polyvinyl alcohol. These polymeric complexes and composite films were characterized by FTIR. The magnetic properties of the complex and its related composite film were measured using a physical property measurement system. It was found that the properties of films are similar to those of their related polymeric complexes. © 2004 Wiley Periodicals, Inc. J Appl Polym Sci 93: 1264–1270, 2004

Co-reporter:Weilin Sun, Liming Jiang, Jian Weng, BingJing He, Zhiquan Shen
Materials Chemistry and Physics 2003 Volume 78(Issue 3) pp:676-683
Publication Date(Web):28 February 2003
DOI:10.1016/S0254-0584(02)00417-0
This paper describes the syntheses, structures and magnetic properties of novel bithiazole based polymeric complexes incorporating ferro ions and hexacyanoferrate groups. The polymer (referred to as SDP) is a condensed product, which obtained from the polycondensation of salicylic acid with 2,2′-diamino-4,4′-bithiazole (DABT) and paraformaldehyde. Its ferro-complex (SDP-Fe2+) reacted with potassium ferricyanide (K3[Fe(CN)6]) in DMSO, producing the polymeric–inorganic complex (SDP-Prussian blue). On the basis of preliminary characterization via spectroscopy techniques, reasonable structures have been proposed for these bithiazole based metallopolymers. The magnetic behavior of the polymeric complexes was measured as a function of magnetic field strength (0–60 kOe) at 5 K and as a function of temperature (5–300 K) at applied fields of 30 and 1000 Oe. SDP-Prussian blue exhibits a hysteresis cycle at 5 K, in which the observed coercive field (HC) is 40 Oe and the remnant magnetization (Mr) is 0.035 emu g−1. The results of measurements indicate that SDP-Fe2+ is an antiferromagnet, while SDP-Prussian blue shows a soft-ferromagnetic behavior.
Glycine, N-(carboxymethyl)-N-[(4-ethenylphenyl)methyl]-
2-Propenoic acid, 2-methyl-, 2-[(8-hydroxy-5-quinolinyl)methoxy]ethyl ester
2-Propenoic acid, 2-methyl-, (4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl ester
Butanedioic acid, 1-[(4S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo-1H-pyrano[3',4':6,7]indolizino[1,2-b]quinolin-9-yl] 4-[2-[(2-methyl-1-oxo-2-propen-1-yl)oxy]ethyl] ester
2-Propenoic acid, 2-methyl-, 4-[2,2':6',2''-terpyridin]-4'-ylphenyl ester
1-Hexanol, 6-[[2,6-bis(1-methyl-1H-benzimidazol-2-yl)-4-pyridinyl]oxy]-
2-Propenoic acid, 6-[[2,6-bis(1-methyl-1H-benzimidazol-2-yl)-4-pyridinyl]oxy]hexyl ester