Citation: TANG Zuwu, LU Shengchang, LIN Xinxing, WU Hui, HUANG Liulian, CHEN Lihui. Research Progress on Catechol-Containing Polymers[J]. Chinese Journal of Applied Chemistry, ;2018, 35(12): 1399-1410. doi: 10.11944/j.issn.1000-0518.2018.12.180012 shu

Research Progress on Catechol-Containing Polymers

College of Material Engineering, Fujian Agriculture and Forestry University, Fuzhou 350002, China

Corresponding author: WU Hui, wuhui@fafu.edu.cn
Received Date: 16 January 2018
Revised Date: 27 February 2018
Accepted Date: 22 March 2018

Fund Project: Technology Cooperation and Exchange Project of Fujian Agriculture and Forestry University KXb16002ASupported by the National Natural Science Foundation of China(No.21774021, No.31470598), the Award Program for Minjiang Scholar Professorship, and Technology Cooperation and Exchange Project of Fujian Agriculture and Forestry University(No.KXb16002A)the Award Program for Minjiang Scholar Professorship the National Natural Science Foundation of China 31470598the National Natural Science Foundation of China 21774021

Figures(7)

Catechol-containing polymers are widely used in the fields of adhesives, hydrogels, biomedicines, antifouling coatings, and self-healing materials due to good compatibility, water resistance, and adhesion.This paper describes the research progress of catechol-containing polymers.The synthesis, structure, and properties of the catechol-containing polymers, as well as its application are summarized.
- adhesion,
- dihydroxyphenylalanine,
- polymer
1. [1]
  Waite J H, Tanzer M L. Polyphenolic Substance of Mytilus Edulis:Novel Adhesive Containing L-Dopa and Hydroxyproline[J]. Science, 1981,212(4498):1038-1040. doi: 10.1126/science.212.4498.1038
2. [2]
  Crisp D J, Walker G, Young G A. Adhesion and Substrate Choice in Mussels and Barnacles[J]. J Colloid Interface Sci, 1985,104(1):40-50. doi: 10.1016/0021-9797(85)90007-4
3. [3]
  Westwood G, Horton T N, Wilker J J. Simplified Polymer Mimics of Cross-Linking Adhesive Proteins[J]. Macromolecules, 2007,40(11):3960-3964. doi: 10.1021/ma0703002
4. [4]
  Faure E, Falentin-Daudre C, Jerome C. Catechols as Versatile Platforms in Polymer Chemistry[J]. Prog Polym Sci, 2013,38(1):236-270. doi: 10.1016/j.progpolymsci.2012.06.004
5. [5]
  Liu Y, Ai K, Lu L. Polydopamine and Its Derivative Materials:Synthesis and Promising Applications in Energy, Environmental, and Biomedical Fields[J]. Chem Rev, 2014,114(9):5057-5115. doi: 10.1021/cr400407a
6. [6]
  Yu M, Hwang J Y, Deming T J. Role of L-3, 4-Dihydroxyphenylalanine in Mussel Adhesive Proteins[J]. J Am Chem Soc, 1999,121(24):5825-5826. doi: 10.1021/ja990469y
7. [7]
  Fant C, Sott K, Elwing H. Adsorption Behavior and Enzymatically or Chemically Induced Cross-Linking of a Mussel Adhesive Protein[J]. Biofouling, 2000,16(2/4):119-132.
8. [8]
  Sever M J, Weisser J T, Monahan J. Metal-Mediated Cross-Linking in the Generation of a Marine-Mussel Adhesive[J]. Angew Chem Int Ed, 2004,43(4):448-450. doi: 10.1002/(ISSN)1521-3773
9. [9]
  Funk C. Synthesis of dl-3:4-Dihydroxyphenylalanine[J]. J Chem Soc Trans, 1911,99:554-557. doi: 10.1039/CT9119900554
10. [10]
  Barry R H, Mattocks A M, Hartung W H. A New Synthesis of 3, 4-Dihydroxyphenylalanine(dopa)[J]. J Am Chem Soc, 1948,70(2):693-694. doi: 10.1021/ja01182a079
11. [11]
  Jiang Z, Liu J, Jin L. Extraction and Application of Perna Viridis Foot Protein as Bioadhesive[J]. J Biomed Eng, 2010,27(6):1266-1273.
12. [12]
  Yoshida H, Tanaka Y, Nakayama K. Production of 3, 4-Dihydroxyphenyl-L-Alanine(L-DOPA) and Its Derivatives by Vibrio tyrosinaticus[J]. Agric Biol Chem, 1973,37(9):2121-2126.
13. [13]
  Nagasaki T, Sugita M, Fukawa H. Studies on the Reaction Conditions of DOPA Production with Alcaligenes Faecalis[J]. Agric Biol Chem, 2008,37(12):2841-2847.
14. [14]
  Ryu B J, Ku S H, Lee H. Mussel-Inspired Polydopamine Coating as a Universal Route to Hydroxyapatite Crystallization[J]. Adv Funct Mater, 2010,20(13):2132-2139. doi: 10.1002/adfm.v20:13
15. [15]
  You I, Kang S M, Lee S. Polydopamine Microfluidic System Toward a Two-Dimensional, Gravity-Driven Mixing Device[J]. Angew Chem Int Ed, 2012,51(25):6126-6130. doi: 10.1002/anie.201200329
16. [16]
  Liu X, Can J, Li J. Mussel-Inspired Polydopamine:A Biocompatible and Ultrastable Coating for Nanoparticles in Vivo[J]. ACS Nano, 2013,7(10):9384-9395. doi: 10.1021/nn404117j
17. [17]
  Shi J, Yang C, Zhang S. Polydopamine Microcapsules with Different Wall Structures Prepared by a Template-Mediated Method for Enzyme Immobilization[J]. ACS Appl Mater Interfaces, 2013,5(20):9991-9997. doi: 10.1021/am403523d
18. [18]
  YANG Xiaotian, SHUAI Xi, LUO Yanmei. Fabrication and Application of the Superhydrophobic Sponge Modified with Poly(dimethylsiloxane)/Silver Micro/Nano-particles/Polydopamine[J]. Chinese J Appl Chem, 2015,32(6):726-732.
19. [19]
  Ni Y, Jiang W, Tong G. Preparation of Polydopamine Nanocapsules in a Miscible Tetrahydrofuran-Buffer Mixture[J]. Org Biomol Chem, 2015,13(3):686-690.
20. [20]
  Daly W H, Moulay S. Synthesis of Poly(vinylcatechols)[J]. J Polym Sci Polym Syp, 1986,74(1):227-242.
21. [21]
  Lim C, Huang J, Kim S. Nanomechanics of Poly(catecholamine) Coatings in Aqueous Solutions[J]. Angew Chem Int Ed, 2016,55(10):3342-3346. doi: 10.1002/anie.201510319
22. [22]
  Guvendiren M, Messersmith P B, Shull K R. Self-Assembly and Adhesion of DOPA-Modified Methacrylic Triblock Hydrogels[J]. Biomacromolecules, 2008,9(1):122-128. doi: 10.1021/bm700886b
23. [23]
  Stepuk A, Halter J G, Schaetz A. Mussel-Inspired Load Bearing Metal-Polymer Glues[J]. Chem Comm, 2012,48(50):6238-6240. doi: 10.1039/c2cc31996a
24. [24]
  Meredith H J, Wilker J J. The Interplay of Modulus, Strength, and Ductility in Adhesive Design Using Biomimetic Polymer Chemistry[J]. Adv Funct Mater, 2015,25(31):5057-5065. doi: 10.1002/adfm.v25.31
25. [25]
  Nishida J, Kobayashi M, Takahara A. Light-Triggered Adhesion of Water-Soluble Polymers with a Caged Catechol Group[J]. ACS Macro Lett, 2013,2:112-115. doi: 10.1021/mz300524q
26. [26]
  Nishida J, Kobayashi M, Takahara A. Gelation and Adhesion Behavior of Mussel Adhesive Protein Mimetic Polymer[J]. J Poly Sci Part A Poly Chem, 2013,51(5):1058-1065. doi: 10.1002/pola.26487
27. [27]
  Xu H, Nishida J, Ma W. Competition Between Oxidation and Coordination in Cross-Linking of Polystyrene Copolymer Containing Catechol Groups[J]. ACS Macro Lett, 2013,1(4)457460.
28. [28]
  Xu H, Nishida J, Wu H. Structural Effects of Catechol-Containing Polystyrene Gels Based on a Dual Cross-Linking Approach[J]. Soft Matter, 2013,9(6):1967-1974. doi: 10.1039/C2SM26994E
29. [29]
  Lee M S, Lee J E, Byun E. Target-Specific Delivery of SiRNA by Stabilized Calcium Phosphate Nanoparticles Using Dopa-Hyaluronic Acid Conjugate[J]. J Control Release, 2014,192(28):122-130.
30. [30]
  You I, Kang S M, Byun Y. Enhancement of Blood Compatibility of Poly(urethane) Substrates by Mussel-Inspired Adhesive Heparin Coating[J]. Bioconjugate Chem, 2011,22(7):1264-1269. doi: 10.1021/bc2000534
31. [31]
  ZHU Liping, XU Youyi, XI Zhenyu. Self-Polymerization of DOPA on Polyethylene Porous Membranes and Immobilization of Heparin[J]. Acta Polym Sin, 2009,1(4):394-397. doi: 10.3321/j.issn:1000-3304.2009.04.017
32. [32]
  Li L, Yan B, Yang J. Novel Mussel-Inspired Injectable Self-healing Hydrogel with Anti-biofouling Property[J]. Adv Mater, 2015,27(7):1294-1299. doi: 10.1002/adma.201405166
33. [33]
  Mattson K M, Latimer A A, Mcgrath A J. A Facile Synthesis of Catechol-Functionalized Poly(ethylene oxide) Block and Random Copolymers[J]. J Polym Sci Part A Polym Chem, 2015,53(23):2685-2692. doi: 10.1002/pola.v53.23
34. [34]
  Niederer K, Schüll C, Leibig D. Catechol Acetonide Glycidyl Ether(CAGE):A Functional Epoxide Monomer for Linear and Hyperbranched Multi-catechol Functional Polyether Architectures[J]. Macromolecules, 2016,49(5):1655-1665. doi: 10.1021/acs.macromol.5b02441
35. [35]
  Lee H, Lee K D, Pyo K B. Catechol-Grafted Poly(ethylene glycol) for PEGylation on Versatile Substrates[J]. Langmuir, 2010,26(6):3790-3793. doi: 10.1021/la904909h
36. [36]
  Wang R, Li J, Chen W. A Biomimetic Mussel-Inspired ε-Poly-l-lysine Hydrogel with Robust Tissue-Anchor and Anti-Infection Capacity[J]. Adv Funct Mater, 2017,27(8)1604894. doi: 10.1002/adfm.v27.8
37. [37]
  Filippidi E, Cristiani T R, Eisenbach C D. Toughening Elastomers Using Mussel-Inspired Iron-Catechol Complexes[J]. Science, 2017,358(6362):502-505. doi: 10.1126/science.aao0350
38. [38]
  TU Xiaoxiong, SUN Peiyu, ZHENG Zhen. Synthesis and Performance of Polyurethane Adhesives Based on Dopamine[J]. J Funct Polym, 2013,26(1):43-49.
39. [39]
  SUN Peiyu, TIAN Liying, ZHENG Zhen. Dopamine-Containing Mussel Mimetic Polyurethane[J]. Acta Polym Sin, 2009,1(8):803-808. doi: 10.3321/j.issn:1000-3304.2009.08.015
40. [40]
  Kim K, Ryu J H, Lee D Y. Bio-Inspired Catechol Conjugation Converts Water-Insoluble Chitosan into a Highly Water-Soluble, Adhesive Chitosan Derivative for Hydrogels and LbL Assembly[J]. Biomater Sci, 2013,1(7):783-790. doi: 10.1039/c3bm00004d
41. [41]
  Yamada K, Chen T, Kumar G. Chitosan Based Water-Resistant Adhesive.Analogy to Mussel Glue[J]. Biomacromolecules, 2000,1(2):252-258. doi: 10.1021/bm0003009
42. [42]
  Karabulut E, Pettersson T, Ankerfors M. Adhesive Layer-by-Layer Films of Carboxymethylated Cellulose Nanofibril Dopamine Covalent Bioconjugates Inspired by Marine Mussel Threads[J]. ACS Nano, 2012,6(6):4731-4739. doi: 10.1021/nn204620j
43. [43]
  Wilker J J. Self-Healing Polymers:Sticky When Wet[J]. Nature Mater, 2014,13(9):849-850. doi: 10.1038/nmat4070
44. [44]
  Li A, Mu Y, Jiang W. A Mussel-Inspired Adhesive with Stronger Bonding Strength under Underwater Conditions than under Dry Conditions[J]. Chem Comm, 2015,51(44):9117-9120. doi: 10.1039/C5CC00101C
45. [45]
  Wilker J J. Positive Charges and Underwater Adhesion[J]. Science, 2015,349(6248):582-583. doi: 10.1126/science.aac8174
46. [46]
  Brennan M J, Kilbride B F, Wilker J J. A Bioinspired Elastin-Based Protein for a Cytocompatible Underwater Adhesive[J]. Biomater, 2017,124:116-125. doi: 10.1016/j.biomaterials.2017.01.034
47. [47]
  Waite J H. Adhesion a la Moule[J]. Integr Comp Biol, 2002,42(6):1172-1180. doi: 10.1093/icb/42.6.1172
48. [48]
  Zhou J, Defante A P, Lin F. Adhesion Properties of Catechol-Based Biodegradable Amino Acid-Based Poly(ester urea) Copolymers Inspired from Mussel Proteins[J]. Biomacromolecules, 2015,16(1):266-274. doi: 10.1021/bm501456g
49. [49]
  Meredith H J, Jenkins C L, Wilker J J. Enhancing the Adhesion of a Biomimetic Polymer Yields Performance Rivaling Commercial Glues[J]. Adv Funct Mater, 2014,24(21):3259-3267. doi: 10.1002/adfm.201303536
50. [50]
  Yavvari P S, Srivastava A. Robust, Self-healing Hydrogels from Catechol Rich Polymers[J]. J Mater Chem B, 2015,3(5):899-910. doi: 10.1039/C4TB01307G
51. [51]
  Krogsgaard M, Behrens M A, Pedersen J S. Self-healing Mussel-Inspired Multi-pH-Responsive Hydrogels[J]. Biomacromolecules, 2013,14(2):297-301. doi: 10.1021/bm301844u
52. [52]
  Jiang J, Zhang P, Zhu L. Improving Antifouling Ability and Hemocompatibility of Poly(vinylidene fluoride) Membranes by Polydopamine-Mediated ATRP[J]. J Mater Chem B, 2015,3(39):7698-7706. doi: 10.1039/C5TB01336D
53. [53]
  Lee H, Dellatore S M, Miller W M. Mussel-Inspired Surface Chemistry for Multifunctional Coatings[J]. Science, 2007,318(5849):426-430. doi: 10.1126/science.1147241
54. [54]
  Watanabe H, Fujimoto A, Jin N. Biobased Polymer Coating Using Catechol Derivative Urushiol[J]. Langmuir, 2016,32(18):4619-4623. doi: 10.1021/acs.langmuir.6b00484
55. [55]
  Wei Q, Achazi K, Liebe H. Mussel-Inspired Dendritic Polymers as Universal Multifunctional Coatings[J]. Angew Chem Int Ed, 2014,53(43):11650-11655. doi: 10.1002/anie.201407113
56. [56]
  Zhang L, Shi J, Jiang Z. Facile Preparation of Robust Microcapsules by Manipulating Metal-Coordination Interaction Between Biomineral Layer and Bioadhesive Layer[J]. ACS Appl Mater Inter, 2011,3(2):597-605. doi: 10.1021/am101184h
57. [57]
  Lin X, Ma W, Wu H. Superhydrophobic Magnetic Poly(DOPAm-co-PFOEA)/Fe₃O₄/Cellulose Microspheres for Stable Liquid Marbles[J]. Chem Comm, 2016,52(9):1895-1898. doi: 10.1039/C5CC08842A
58. [58]
  Hong S, Na Y S, Choi S. Non-covalent Self-assembly and Covalent Polymerization Co-contribute to Polydopamine Formation[J]. Adv Funct Mater, 2012,22(22):4711-4717. doi: 10.1002/adfm.v22.22
59. [59]
  Wei Q, Zhang F, Li J. Oxidant-induced Dopamine Polymerization for Multifunctional Coatings[J]. Polym Chem, 2010,1:1430-1433. doi: 10.1039/c0py00215a
60. [60]
  Lee H, Rho J, Messersmith P B. Facile Conjugation of Biomolecules onto Surfaces via Mussel Adhesive Protein Inspired Coatings[J]. Adv Mater, 2009,21(4):431-434. doi: 10.1002/adma.v21:4
61. [61]
  Lv Y, Du Y, Chen Z. Nanocomposite Membranes of Polydopamine/Electropositive Nanoparticles/Polyethyleneimine for Nanofiltration[J]. J Membr Sci, 2017,545:99-106.
62. [62]
  Cui S, Kang X, Cai W. Revealing the Formation Mechanism of Insoluble Polydopamine by Using a Simplified Model System[J]. Polym Chem, 2017,8(5):860-865. doi: 10.1039/C6PY02005D
63. [63]
  Lee B P, Messersmith P B, Israelachvili J N. Mussel-Inspired Adhesives and Coatings[J]. Annu Rev Mater Res, 2011,41(1):99-132.
64. [64]
  Zhang H, Zhao T, Newland B. Catechol Functionalized Hyperbranched Polymers as Biomedical Materials[J]. Prog Polym Sci, 2018,78:47-55. doi: 10.1016/j.progpolymsci.2017.09.002
65. [65]
  XIE Dandan, YAN Liang, YIN Yuli. Preparation and Application of Magnetic Multi-ion Imprinted Polymers Based on Multiwalled Carbon Nanotubes[J]. Chinese J Appl Chem, 2017,34(4):456-463.
66. [66]
  Okay O. Macroporous Copolymer Networks[J]. Prog Polym Sci, 2000,25(6):711-779. doi: 10.1016/S0079-6700(00)00015-0
67. [67]
  Yavvari P S, Srivastava A. Robust, Self-healing Hydrogels Synthesised from Catechol Rich Polymers[J]. J Mater Chem B, 2015,3(5):899-910. doi: 10.1039/C4TB01307G
68. [68]
  Lin X, Wa M, Wu H. Fabrication of Cellulose Based Superhydrophobic Microspheres for the Production of Magnetically Actuatable Smart Liquid Marbles[J]. J Bioresour Bioprod, 2017,2(3):110-115.
69. [69]
  Wu H, Higaki Y, Takahara A. Molecular Self-assembly of One-Dimensional Polymer Nanostructures in Nanopores of Anodic Alumina Oxide Templates[J]. Prog Polym Sci, 2018,77:95-117. doi: 10.1016/j.progpolymsci.2017.10.004
70. [70]
  Kaneko D, Wang S, Matsumoto K. Mussel-Mimetic Strong Adhesive Resin from Bio-base Polycoumarates[J]. Polym J, 2011,43(10):855-858. doi: 10.1038/pj.2011.77
71. [71]
  Yang J, Keijsers J, Heek M V. Effect of Molecular Composition and Crosslinking on Adhesion of a Bio-inspired Adhesive[J]. Polym Chem, 2015,6(16):3121-3130. doi: 10.1039/C4PY01790K
72. [72]
  Mu Y, Wan X. Simple but Strong:A Mussel-Inspired Hot Curing Adhesive Based on Polyvinyl Alcohol Backbone[J]. Macromol Rapid Comm, 2016,37(6):545-550. doi: 10.1002/marc.201500723
73. [73]
  Jia M, Li A, Mu Y. Synthesis and Adhesive Property Study of Polyoxetanes Grafted with Catechols via Cu(Ⅰ)-Catalyzed Click Chemistry[J]. Polymer, 2014,55(5):1160-1166. doi: 10.1016/j.polymer.2014.01.028
74. [74]
  Wang X, Liu J, Gao T. Self-Assembly of Catecholic Macroinitiator on Various Substrates and Surface-Initiated Polymerization[J]. Langmuir, 2012,28(5):2574-2581. doi: 10.1021/la204568d
75. [75]
  Zhang C, Ma M, Chen T. Dopamine-Triggered One-Step Polymerization and Co-Deposition of Acrylate Monomers for Functional Coatings[J]. ACS Appl Mater Interfaces, 2017,9(39):34356-34366. doi: 10.1021/acsami.7b11092
76. [76]
  Li G, Yang P, Yang L. Tailoring of the Titanium Surface by Immobilization of Heparin/Fibronectin Complexes for Improving Blood Compatibility and Endothelialization:An in Vitro Study[J]. Biomacromolecules, 2011,12(4):1155-1168. doi: 10.1021/bm101468v
77. [77]
  Moon R J, Martini A, Nairn J. Cellulose Nanomaterials Review:Structure, Properties and Nanocomposites[J]. Chem Soc Rev, 2011,40(7):3941-3994. doi: 10.1039/c0cs00108b
78. [78]
  Zhou X, Lin X, White K L. Effect of the Degree of Substitution on the Hydrophobicity of Acetylated Cellulose for Production of Liquid Marbles[J]. Cellulose, 2016,23(1):811-821.
79. [79]
  Tang Z, Li W, Lin X. TEMPO-Oxidized Cellulose with High Degree of Oxidation[J]. Polymers, 2017,9(9)421.
80. [80]
  Wu H, Wu L, Lu S. Robust Superhydrophobic and Superoleophilic Filter Paper via Atom Transfer Radical Polymerization for Oil/Water Separation[J]. Carbohydr Polym, 2018,181:419-425. doi: 10.1016/j.carbpol.2017.08.078
81. [81]
  Forooshani P K, Lee B P. Recent Approaches in Designing Bioadhesive Materials Inspired by Mussel Adhesive Protein[J]. J Polym Sci Part A Polym Chem, 2017,55(1):9-33. doi: 10.1002/pola.v55.1
82. [82]
  Zhang X, Yi J, Zhao G. Layer-by-Layer Assembly of Silver Nanoparticles Embedded Polyelectrolyte Multilayer on Magnesium Alloy with Enhanced Antibacterial Property[J]. Surf Coat Technol, 2016,286:103-112. doi: 10.1016/j.surfcoat.2015.12.018
83. [83]
  Wang B, Jeon Y S, Park H S. Mussel-Mimetic Self-healing Polyaspartamide Derivative Gel via Boron-Catechol Interactions[J]. Express Polym Lett, 2015,9(9):799-808. doi: 10.3144/expresspolymlett.2015.75
1. [1]
  Zhongxin YU , Wei SONG , Yang LIU , Yuxue DING , Fanhao MENG , Shuju WANG , Lixin YOU . Fluorescence sensing on chlortetracycline of a Zn-coordination polymer based on mixed ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(12): 2415-2421. doi: 10.11862/CJIC.20240304
2. [2]
  Bao Jia , Yunzhe Ke , Shiyue Sun , Dongxue Yu , Ying Liu , Shuaishuai Ding . Innovative Experimental Teaching for the Preparation and Modification of Conductive Organic Polymer Thin Films in Undergraduate Courses. University Chemistry, 2024, 39(10): 271-282. doi: 10.12461/PKU.DXHX202404121
3. [3]
  Xiao SANG , Qi LIU , Jianping LANG . Synthesis, structure, and fluorescence properties of Zn(Ⅱ) coordination polymers containing tetra-alkenylpyridine ligands. Chinese Journal of Inorganic Chemistry, 2024, 40(11): 2124-2132. doi: 10.11862/CJIC.20240158
4. [4]
  Junjie Zhang , Yue Wang , Qiuhan Wu , Ruquan Shen , Han Liu , Xinhua Duan . Preparation and Selective Separation of Lightweight Magnetic Molecularly Imprinted Polymers for Trace Tetracycline Detection in Milk. University Chemistry, 2024, 39(5): 251-257. doi: 10.3866/PKU.DXHX202311084
5. [5]
  Xingchao Zhao , Xiaoming Li , Ming Liu , Zijin Zhao , Kaixuan Yang , Pengtian Liu , Haolan Zhang , Jintai Li , Xiaoling Ma , Qi Yao , Yanming Sun , Fujun Zhang . 倍增型全聚合物光电探测器及其在光电容积描记传感器上的应用. Acta Physico-Chimica Sinica, 2025, 41(1): 2311021-. doi: 10.3866/PKU.WHXB202311021
6. [6]
  You Wu , Chang Cheng , Kezhen Qi , Bei Cheng , Jianjun Zhang , Jiaguo Yu , Liuyang Zhang . ZnO/D-A共轭聚合物S型异质结高效光催化产H₂O₂及其电荷转移动力学研究. Acta Physico-Chimica Sinica, 2024, 40(11): 2406027-. doi: 10.3866/PKU.WHXB202406027
7. [7]
  .
  南开大学师唯/华北电力大学（保定）刘景维：二维配位聚合物中有序的亲锂冠醚位点用于无枝晶锂沉积
  . CCS Chemistry, 2025, 7(0): -.
8. [8]
  Liang TANG , Jingfei NI , Kang XIAO , Xiangmei LIU . Synthesis and X-ray imaging application of lanthanide-organic complex-based scintillators. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1892-1902. doi: 10.11862/CJIC.20240139
9. [9]
  Xin MA , Ya SUN , Na SUN , Qian KANG , Jiajia ZHANG , Ruitao ZHU , Xiaoli GAO . A Tb₂ complex based on polydentate Schiff base: Crystal structure, fluorescence properties, and biological activity. Chinese Journal of Inorganic Chemistry, 2024, 40(7): 1347-1356. doi: 10.11862/CJIC.20230357
10. [10]
  Xinyu Liu , Weiran Hu , Zhengkai Li , Wei Ji , Xiao Ni . Algin Lab: Surging Luminescent Sea. University Chemistry, 2024, 39(5): 396-404. doi: 10.3866/PKU.DXHX202312021
11. [11]
  Xiyuan Su , Zhenlin Hu , Ye Fan , Xianyuan Liu , Xianyong Lu . Change as You Want: Multi-Responsive Superhydrophobic Intelligent Actuation Material. University Chemistry, 2024, 39(5): 228-237. doi: 10.3866/PKU.DXHX202311059
12. [12]
  Zongpei Zhang , Yanyang Li , Yanan Si , Kai Li , Shuangquan Zang . Developing a Chemistry Experiment Center Employing a Multifaceted Approach to Serve High-Quality Laboratory Education. University Chemistry, 2024, 39(7): 13-19. doi: 10.12461/PKU.DXHX202404041
13. [13]
  Ruilin Han , Xiaoqi Yan . Comparison of Multiple Function Methods for Fitting Surface Tension and Concentration Curves. University Chemistry, 2024, 39(7): 381-385. doi: 10.3866/PKU.DXHX202311023
14. [14]
  Xingyuan Lu , Yutao Yao , Junjing Gu , Peifeng Su . Energy Decomposition Analysis and Its Application in the Many-Body Effect of Water Clusters. University Chemistry, 2025, 40(3): 100-107. doi: 10.12461/PKU.DXHX202405074
15. [15]
  Li'na ZHONG , Jingling CHEN , Qinghua ZHAO . Synthesis of multi-responsive carbon quantum dots from green carbon sources for detection of iron ions and L-ascorbic acid. Chinese Journal of Inorganic Chemistry, 2025, 41(4): 709-718. doi: 10.11862/CJIC.20240280
16. [16]
  Conghao Shi , Ranran Wang , Juli Jiang , Leyong Wang . The Illustration on Stereoisomers of Macrocycles Containing Multiple Chiral Centers via Tröger Base-based Macrocycles. University Chemistry, 2024, 39(7): 394-397. doi: 10.3866/PKU.DXHX202311034
17. [17]
  Pengcheng Yan , Peng Wang , Jing Huang , Zhao Mo , Li Xu , Yun Chen , Yu Zhang , Zhichong Qi , Hui Xu , Henan Li . Engineering Multiple Optimization Strategy on Bismuth Oxyhalide Photoactive Materials for Efficient Photoelectrochemical Applications. Acta Physico-Chimica Sinica, 2025, 41(2): 100014-. doi: 10.3866/PKU.WHXB202309047
18. [18]
  Jiajia Li , Xiangyu Zhang , Zhihan Yuan , Zhengyang Qian , Jian Zhu . 3D Printing Based on Photo-Induced Reversible Addition-Fragmentation Chain Transfer Polymerization. University Chemistry, 2024, 39(5): 11-19. doi: 10.3866/PKU.DXHX202309073
19. [19]
  Zijian Zhao , Yanxin Shi , Shicheng Li , Wenhong Ruan , Fang Zhu , Jijun Jiang . A New Exploration of the Preparation of Polyacrylic Acid by Free Radical Polymerization Based on the Concept of Green Chemistry. University Chemistry, 2024, 39(5): 315-324. doi: 10.3866/PKU.DXHX202311094
20. [20]
  Xiaowei TANG , Shiquan XIAO , Jingwen SUN , Yu ZHU , Xiaoting CHEN , Haiyan ZHANG . A zinc complex for the detection of anthrax biomarker. Chinese Journal of Inorganic Chemistry, 2024, 40(10): 1850-1860. doi: 10.11862/CJIC.20240173

Get Citation

PDF

XML

Metrics

PDF Downloads(107)
Abstract views(3980)
HTML views(1696)

通讯作者: 陈斌, bchen63@163.com

1.
沈阳化工大学材料科学与工程学院沈阳 110142

Research Progress on Catechol-Containing Polymers

南开大学师唯/华北电力大学（保定）刘景维：二维配位聚合物中有序的亲锂冠醚位点用于无枝晶锂沉积

Metrics

通讯作者: 陈斌, bchen63@163.com