RING-OPENING POLYMERIZAION OF 2,2-DIMETHYLTRIMETHYLENE CARBONATE INITIATED BY IN SITU GENERATED, TETRAHYDROSALEN STABLIZED YTTRIUM BOROHYDRIDE COMPLEX AND RANDOM COPOLYMERIZATION WITH e-CAPROLACTONE
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RING-OPENING POLYMERIZAION OF 2,2-DIMETHYLTRIMETHYLENE CARBONATE INITIATED BY IN SITU GENERATED, TETRAHYDROSALEN STABLIZED YTTRIUM BOROHYDRIDE COMPLEX AND RANDOM COPOLYMERIZATION WITH e-CAPROLACTONE
Chinese Journal of Polymer ScienceVol. 29, Issue 3, Pages: 390-396(2011)
Affiliations:
Key Laboratory of Macromolecule Synthesis and Functionalization, Ministry of EducationDepartment of Polymer Science and Engineering, Zhejiang University, Hangzhou 310027, China
Author bio:
**Wei-lin Sun (孙维林), E-mail: opl_sunwl@emb.zju.edu.cn
Jing Huang, Jian-fang Yu, Han-jian Yu, et al. RING-OPENING POLYMERIZAION OF 2,2-DIMETHYLTRIMETHYLENE CARBONATE INITIATED BY IN SITU GENERATED, TETRAHYDROSALEN STABLIZED YTTRIUM BOROHYDRIDE COMPLEX AND RANDOM COPOLYMERIZATION WITH e-CAPROLACTONE[J]. Chinese Journal of Polymer Science, 2011, 29(3): 390-396.
DOI:
Jing Huang, Jian-fang Yu, Han-jian Yu, et al. RING-OPENING POLYMERIZAION OF 2,2-DIMETHYLTRIMETHYLENE CARBONATE INITIATED BY IN SITU GENERATED, TETRAHYDROSALEN STABLIZED YTTRIUM BOROHYDRIDE COMPLEX AND RANDOM COPOLYMERIZATION WITH e-CAPROLACTONE[J]. Chinese Journal of Polymer Science, 2011, 29(3): 390-396.DOI: 10.1007/s10118-011-1044-8.
RING-OPENING POLYMERIZAION OF 2,2-DIMETHYLTRIMETHYLENE CARBONATE INITIATED BY IN SITU GENERATED, TETRAHYDROSALEN STABLIZED YTTRIUM BOROHYDRIDE COMPLEX AND RANDOM COPOLYMERIZATION WITH e-CAPROLACTONE
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℃
toluene: 0.5 mL
DTC: 0.6 g
PDTC with
M
n
= 15600 and PDI = 2.15 was obtained. Through
1
H-NMR and
13
C-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 CL-DTC
which were determined by the specific signals in
1
H-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.
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