浏览全部资源
扫码关注微信
1.国家有机毒物控制与资源化工程技术研究中心 南京大学环境学院 南京 210023
2.吸附与分离功能高分子材料教育部重点实验室 南开大学高分子化学研究所 天津 300071
Published:2018-7,
Received:1 February 2018,
Revised:5 April 2018,
扫 描 看 全 文
Zi-yu Wang, Wen-wen He, Yun-long Xu, Wei Huang, Wei Jiang, Hong Li, Quan-xing Zhang. Controlled Synthesis of PLA-series Environment-friendly Polymers with Guanidine Catalysts. [J]. Acta Polymerica Sinica 0(7):786-796(2018)
Zi-yu Wang, Wen-wen He, Yun-long Xu, Wei Huang, Wei Jiang, Hong Li, Quan-xing Zhang. Controlled Synthesis of PLA-series Environment-friendly Polymers with Guanidine Catalysts. [J]. Acta Polymerica Sinica 0(7):786-796(2018) DOI: 10.11777/j.issn1000-3304.2018.18036.
可控聚合反应是进行大分子结构设计及获得优异性能聚合物的重要手段. 作者近年来设计合成/筛选了若干种无毒有机胍化合物作为催化剂/引发剂,实现了可控缩聚、开环聚合、解聚反应. 以生物质有机胍肌酐(CR)为催化剂实现了L-/D-乳酸(LLa/DLa)的等规熔融缩聚(Iso-MP),高产率(85%)合成得到了高等规度聚L-/D-乳酸(PLLA、PDLA,Iso.
>
98%);以CR催化Iso-MP反应得的中分子量聚L-/D-乳酸(
M
w
= 2.2 × 10
4
,Iso. = 98.2%)为原料经熔融-固相缩聚(MP-SSP)联用法合成得到高分子量、高等规度PLLA、PDLA (
M
w
= 1.0 × 10
5
,Iso.
>
98%),聚合物热分解温度(
T
d
i
= 324.3 °C)较SnCl
2
·2H
2
O催化法合成聚合物高120 °C;由CR催化LLa/DLa的Iso-MP及其后解聚反应合成得到了光学纯L-/D-丙交酯(LLA、DLA,
e.e.
100%),副产的聚合物残渣
r
-PLLA/
r
-PDLA经水解后循环用作LLA/DLA合成原料,光学纯LLA/DLA总产率达到98%. 设计合成了数种位阻型有机胍羧酸盐(HBG·OAc、CRA、CRG、CRL、TBDA),表征了其分子结构,用以实现LLA的活性开环聚合. 合成了单一光学构型的L-乳酸-L-丝氨酸吗啉二酮(3
S
6
S
-BMMD),测定了其单晶分子结构并以CRA为引发剂进行了3
S
6
S
-BMMD的活性开环聚合,聚合物经脱保护后合成得到双亲功能基化生物降解聚合物聚(L-乳酸-L-丝氨酸). 采用
1
H-NMR、
13
C-NMR跟踪监测法表征了大分子物种的精细结构,推断了上述可控反应的机理.
Controlled polymerization is of great significance for the tailoring of macromolecular structure and synthesis of polymers with excellent properties. Several non-toxic organic guanidinines were prepared/selected in our laboratory in recent years and used as the catalysts/initiators to realize controlled melt polycondensation (MP)
ring-opening polymerization (ROP)
and depolymerization (DEP). Isotactic melt polycondensation (Iso-MP) of L-lactic acid/D-lactic acid (LLa/DLa) was carried out for the first time with biogenic creatinine (CR) catalyst and poly(L-lactic acid)/poly(D-lactic acid) (PLLA/PDLA) with high isotacticity (Iso.
>
98%) was obtained; Combined MP with solid-state polycondensation (MP-SSP) of the medium molecular weight PLLA/PDLA (
M
w
= 2.2 × 10
4
Iso. = 98.2%)
prepared by the Iso-MP with CR
was carried out
and high molecular weight PLLA/PDLA (
M
w
>
1.0 × 10
5
) with high isotacticity (Iso.
>
98%) was obtained. The initial decomposition temperature (
T
d
i
) of the synthesized PLLA reached up to 324.5 °C
which was 120 °C higher than that of PLLA synthesized by SnCl
2
·2H
2
O catalyst; Optical pure (
e.e.
100%) L-lactide/D-lactide (OP-LLA/OP-DLA) were synthesized
via
Iso-MP and the subsequent depolymerization (DEP) of LMW-PLLA/LMW-PDLA (
M
w
= 8.0 × 10
2
– 9.0 × 10
2
) with CR catalyst. The polymer residues (
r
-PLLA/
r
-PDLA)
produced accompanying with the lactides formation
were reused as the raw material for LLA/DLA synthesis after being hydrolyzed. The total yield of OP-LLA/OP-DLA reached up to 98%; Several sterically hindered guanidine carboxylates (HBG·OAc
CRA
CRG
CRL
TBDA) were synthesized and used to realize living ROP of LLA. An optical pure morpholine-2
5-dione (3
S
6
S
-BMMD)
derived from LLa and L-serine
was synthesized. Living ROP of 3
S
6
S
-BMMD was carried out with CRA catalyst for the first time. After debenzylation of the synthesized P(3
S
6
S
-BMMD)
an amphiphillic copolymer P(LLa-
co
-Ser) was obtained
which is a useful support material in biomedical areas. The fine molecular structures and isotacticities of growing polymeric species were characterized by
in situ
monitoring with
1
H-NMR
13
C-NMR. And the mechanisms of the above mentioned controlled polymerizations were proposed.
有机胍立构专一性缩聚活性开环聚合环境友好聚合物
Organic guanidineIsotactic polycondensationLiving ring-opening polymerizationEnvironment-friendly polymers
Zhang Quanxing(张全兴). Science & Technology Review(科技导报), 2012, 30(18): 3
Auras R, Lim L T, Selke S E M, Tsuji H, eds. Poly(lactic acid): Synthesis, Structures, Properties, Processing, and Applications. Hoboken, New Jersey: John Wiley & Sons, Inc. 2010. 499
Jhurry D, Bhaw-Luximon A, Spassky N . Macromol Symp , . 2001 . 175 67 - 79.
Chamberlain B M, Cheng M, Moore D R, Ovitt T M, Lobkovsky E B, Coates G W . J Am Chem Soc , . 2001 . 123 ( 14 ): 3229 - 3238.
Zhong Z, Dijkstra P J, Feijen J . J Am Chem Soc , . 2003 . 125 ( 37 ): 11291 - 11298.
O'Keefe B J, Hillmyer M A, Tolman W B . J Chem Soc, Dalton Trans , . 2001 . ( 15 ): 2215 - 2224.
Doherty S, Errington R J, Housley N, Clegg W . Organometallics , . 2004 . 23 ( 10 ): 2382 - 2388.
Ovitt T M, Coates G W . J Am Chem Soc , . 2002 . 124 ( 7 ): 1316 - 1326.
Dechy-Cabaret O, Martin-Vaca B, Bourissou D . Chem Rev , . 2004 . 104 ( 12 ): 6147 - 6176.
Sun J, Shi W, Chen D, Liang C . J Appl Polym Sci , . 2002 . 86 ( 13 ): 3312 - 3315.
Kricheldorf H R, Hachmann-Thiessen H, Schwarz G . Biomacromolecules , . 2004 . 5 ( 2 ): 492 - 496.
Kricheldorf H R . Chemosphere , . 2001 . 43 ( 1 ): 49 - 54.
Kricheldorf H R, Rost S . Polymer , . 2005 . 46 ( 10 ): 3248 - 3256.
Mazarro R, de Lucas A, Gracia I, Rodriguez J F . J Biomed Mater Res, Part B , . 2008 . 85B ( 1 ): 196 - 203.
Tanzi M C, Verderio P, Lampugnani M G, Resnati M, Dejana E, Sturani E . J Mater Sci: Mater Med , . 1994 . 5 ( 6 ): 393 - 396.
Kim K W, Woo S I . Macromol Chem Phys , . 2002 . 203 ( 15 ): 2245 - 2250.
Moon S I, Lee C W, Miyamoto M, Kimura Y . J Polym Sci, Part A: Polym Chem , . 2000 . 38 ( 9 ): 1673 - 1679.
Jiang W, Huang W, Cheng N, Qi Y, Zong X, Li H, Zhang Q . Polymer , . 2012 . 53 ( 24 ): 5476 - 5479.
Gros P, Le Perchec P, Senet J P . J Org Chem , . 1994 . 59 ( 17 ): 4925 - 4930.
Moon S I, Lee C W, Taniguchi I, Miyamoto M, Kimura Y . Polymer , . 2001 . 42 ( 11 ): 5059 - 5062.
Huang W, Cheng N, Qi Y, Zhang T, Jiang W, Li H, Zhang Q . Polymer , . 2014 . 55 ( 6 ): 1491 - 1496.
Nishida H, Mori T, Hoshihara S, Fan Y, Shirai Y, Endo T . Polym Degrad Stab , . 2003 . 81 ( 3 ): 515 - 523.
Dantas F J S, Moraes M O, Mattos J C P d, Bezerra R J A C, Carvalho E F, Filho M B, Araújo A C d . Toxicol Lett , . 1999 . 110 ( 3 ): 129 - 136.
Dantas F J S, Mattos J C P d, Moraes M O, Viana M E, Lage C A S, Cabral-Neto J B, Leitão A C,Bernardo-Filho M, Bezerra R J A C, Carvalho J J, Caldeira-de-Araújo A . Food Chem Toxicol , . 2002 . 40 ( 10 ): 1493 - 1498.
Guedes A P, Cardoso V N, De Mattos J C, Dantas F J, Matos V C, Silva J C, Bezerra R J, Caldeira-de-Araujo A . Nucl Med Biol , . 2006 . 33 ( 7 ): 915 - 921.
Huang W, Qi Y, Cheng N, Zong X, Zhang T, Jiang W, Li H, Zhang Q . Polym Degrad Stab , . 2014 . 101 18 - 23.
Sheng Jiaye(盛家业), Wang Ziyu(王子羽), Xu Yunlong(徐云龙), Huang Wei(黄伟), Jiang Wei(江伟), Li Hong(李弘), Zhang Quanxing(张全兴). Ion Exchange and Adsorption(离子交换与吸附), 2017, (3): 193-202
Wang C, Li H, Zhao X . Biomaterials , . 2004 . 25 ( 27 ): 5797 - 5801.
Li H, Wang C, Jin Y, Zhao X, Feng B . J Polym Sci, Part A: Polym Chem , . 2004 . 42 ( 15 ): 3775 - 3781.
Li Hong(李弘), Zhang Saihui(张赛晖), Jiao Zhifeng(焦志峰), Zuo Jiaqin(左佳卿). Acta Polymerica Sinica(高分子学报), 2008, (7): 667-672
Li H, Zhang S, Jiao J, Jiao Z, Kong L, Xu J, Li J, Zuo J, Zhao X . Biomacromolecules , . 2009 . 10 ( 5 ): 1311 - 1314.
Li Hong(李弘), Jiao Jieping(焦洁平), Kong Lijun(孔丽君), Jiao Zhifeng(焦志峰), Zhang Donglai(张东来), Xu Jie(徐杰), He Peiru(何培茹). Chinese Journal of Organic Chemistry(有机化学), 2009, 29(5): 736-741
Barrera D A, Zylstra E, Lansbury P T, Langer R . Macromolecules , . 1995 . 28 ( 2 ): 425 - 432.
Feng Y, Klee D, Keul H, Hocker H . Macromol Chem Phys , . 2000 . 201 ( 18 ): 2670 - 2675.
Wang D, Feng X D . Macromolecules , . 1997 . 30 ( 19 ): 5688 - 5692.
Chisholm M H, Galucci J, Krempner C, Wiggenhorn C . Dalton Trans , . 2006 . 0 846 - 851.
Barrera D A, Zylstra E, Lansbury P T, Langer R . Macromolecules , . 1995 . 28 ( 2 ): 425 - 432.
Pang Z, Li H, He P, Wang Y, Ren H, Wang H, Zhu X X . J Polym Sci, Part A: Polym Chem , . 2012 . 50 ( 19 ): 4004 - 4009.
Lohmeijer B G G, Pratt R C, Leibfarth F, Logan J W, Long D A, Dove A P, Nederberg F, Choi J, Wade C, Waymouth R M, Hedrick J L . Macromolecules , . 2006 . 39 ( 25 ): 8574 - 8583.
Martello M T, Burns A, Hillmyer M . ACS Macro Lett , . 2012 . 1 ( 1 ): 131 - 135.
Li Hong(李弘), Kong Lijun(孔丽君), Zong Xupeng(宗绪鹏), Jiao Jieping(焦洁平). China Patent(中国发明专利), ZL 200810053913.4. 2011-11-03
Nederberg F, Connor E F, Moller M, Glauser T, Hedrick J L . Angew Chem Int Ed , . 2001 . 40 ( 14 ): 2712 - 2715.
Dove A P, Pratt R C, Lohmeijer B G G, Waymouth R M, Hedrick J L . J Am Chem Soc , . 2005 . 127 ( 40 ): 13798 - 13799.
Coulembier O, Mespouille L, Hedrick J L, Waymouth R M, Dubois P . Macromolecules , . 2006 . 39 ( 12 ): 4001 - 4008.
Connor E, Nyce G W, Myers M, Mock A, Hedrick J L . J Am Chem Soc , . 2002 . 124 ( 6 ): 914 - 915.
Zhang L, Nederberg F, Messman J M, Pratt R C, Hedrick J L, Wade C G . J Am Chem Soc , . 2007 . 129 ( 42 ): 12610 - 12611.
Coady D J, Engler A C, Horn H W, Bajjuri K M, Fukushima K, Jones G O, Nelson A, Rice J E, Hedrick J L . ACS Macro Lett , . 2012 . 1 ( 1 ): 19 - 22.
Coady D J, Fukushima K, Horn H W, Rice J E, Hedrick J L . Chem Commun , . 2011 . 47 ( 11 ): 3105 - 3107.
Dove A P, Li H, Pratt R C, Lohmeijer B G G, Culkin D A, Waymouth R M, Hedrick J L . Chem Commun , . 2006 . 0 ( 27 ): 2881 - 2883.
Coulembier O, Lohmeijer B G G, Dove A P, Pratt R C, Mespouille L, Culkin D A, Benight S J, Dubois P, Waymouth R M, Hedrick J L . Macromolecules , . 2006 . 39 ( 17 ): 5617 - 5628.
Dechy-Cabaret O, Martin-Vaca B, Bourissou D . Chem Rev , . 2004 . 104 ( 12 ): 6147 - 6176.
Bai Feng(白峰), Li Hong(李弘). Chinese Journal of Organic Chemistry(有机化学), 2004, 24(12): 1532-1541
Li Hong(李弘). Synthesis of biodegradable polymer using organic catalysts(有机催化剂法可控合成生物降解聚合物). In: Dong Jianhua(董建华) ed. Frontiers and Advances in Polymer Science II(高分子科学前沿与进展II). Beijing(北京): China Science Publishing & Media Ltd.(科学出版社), 2009. 54
Woo H G, Li H. Advanced Functional Materials. Berlin, Heidelberg: Springer, 2011. 227
0
Views
33
下载量
4
CSCD
Publicity Resources
Related Articles
Related Author
Related Institution