SIOC 中文
CJOG
Adv search

Chinese Journal of Organic Chemistry >

2021 , Vol. 41 >Issue 4: 1319 - 1336

DOI: https://doi.org/10.6023/cjoc202007063

REVIEWS

Research Progress of Cellulose and Its Derivatives Supported Copper Catalyst Catalyzed Organic Reactions

  • Xin Chen ,
  • Chunxia Chen ,
  • Jinsong Peng
Expand
  • a College of Chemistry, Chemical Engineering and Resource Utilization, Northeast Forestry University, Harbin 150040
    b Material Science and Engineering College, Northeast Forestry University, Harbin 150040
* Corresponding authors. E-mail: ;
E-mail:

Received date: 2020-07-28

  Revised date: 2020-10-23

  Online published: 2020-11-19

Supported by

Natural Science Foundation of Heilongjiang Province(LC2018003); Fundamental Research Funds for the Central Universities(2572019CG06)

Fold

Abstract

Cellulose, the most abundant natural polymer in nature, is found in vascular plant, cotton, algae and bacteria, and it can be widely employed in organic synthesis and catalytic chemistry as a loading material for metal nanoparticles. In modern times, the field of transition metal catalysis has been developed rapidly, but it has the disadvantages of high cost, difficulty of separation and non-recyclable reuse, thus more and more researchers use cellulose and its derivatives to carry out heterogeneous catalysis. From an economic and efficient point of view, cheap cellulose and its derivatives-loaded copper particles can not only participate in various types of organic conversion efficiently, but also can be recycled and reused many times, thus solving many disadvantages of homogeneous catalysts and achieving green process. The organic reactions catalyzed by different types of cellulose-supported copper catalysts are reviewed, including the construction of C—X bond, cycloaddition, oxidation, reduction, photocatalytic degradation and electrocatalysis. It will promote the application of cellulose and its derivatives-sup- ported catalysts in the future.

Key words： cellulose-supported copper catalyst; functional cellulose; synthesis; organic reaction; heterogeneous catalysis

Cite this article

Xin Chen , Chunxia Chen , Jinsong Peng . Research Progress of Cellulose and Its Derivatives Supported Copper Catalyst Catalyzed Organic Reactions[J]. Chinese Journal of Organic Chemistry, 2021 , 41(4) : 1319 -1336 . DOI: 10.6023/cjoc202007063

References

[1]
Shaghaleh, H.; Xu, X.; Wang, S. RSC Adv. 2018, 8,825.
[2]
Qiu, X.; Hu, S. Materials 2013, 6,738.
[3]
McNamara, J.T.; Morgan, J.L. W.; Zimmer, J. Annu. Rev. Biochem. 2015, 84,895.
[4]
Brett, C.T. Int. Rev. Cytol. 2000, 199,161.
[5]
Wu, X.; Lu, C.; Zhang, W.; Yuan, G.; Xiong, R.; Zhang, X. J. Mater. Chem. 2013, 30,8645.
[6]
Wu, X.; Lu, C.; Zhang, W.; Guan, G.; Xiong, R.; Zhang, X. Environ. Sci.: Nano 2014, 1,71.
[7]
Zhou, Z.; Lu, C.; Wu, X.; Zhang, X. RSC Adv. 2013, 48,26066.
[8]
Klemm, D.; Heublein, B.; Fink, H.P.; Bohn, A. Angew. Chem., Int. Ed. 2005, 44,3358.
[9]
Varshney, K.; Naithani, S. In Cellulose Fibers:Bio- and Nano-Polymer Composites, Green Chemistry and Technology, Eds.: Kalia, S.; Kaith, B.S.;Kaur. I., Springer Science & Business Media, New York, 2011, pp.43~60.
[10]
Saliba, R.; Gauthier, H.; Gauthier, R.; Ramel, M.P. J. Appl. Polym. Sci. 2000, 75,1624.
[11]
Bang, H.; Ma, K.; Devarayan, K.; Kang, C.; Kim, B.; Gopiraman, M.; Kim, I. J. Mater. Sci. Technol. 2016, 32,605.
[12]
Eivazihollagha, A.; B?ckstr?mb, J.; Dahlstr?ma, C.; Carlssonc, F.; Ibrahema, I.; Lindmana, B.; Edlunda, H.; Norgren, M. Mater. Lett. 2017, 187,170.
[13]
Jilal, I.; Barkany, S.E.; Bahari, Z.; Sundman, O.; Loutou, M.; Amhamdi, H. Cellulose 2018, 25,4375.
[14]
Yingkong, P.; Tanskul, S. J. Polym. Environ. 2019, 27,1948.
[15]
Li, Z.; Hori, N.; Takemura, A. Cellulose 2019, 6,2839.
[16]
Reddy, K.R.; Kumar, N.S.; Sreedhar, B.; Kantam, M.L. J. Mol. Catal. A: Chem. 2006, 252,136.
[17]
Reddy, K.R.; Kumar, N.S. Synlett 2006,2246.
[18]
Zhai, X.; Han, S.; Wei, P. Chem. Reagents 2010, 32,397. (in Chinese)
[18]
( 瞿晓璐, 韩世清, 韦萍, 化学试剂, 2010, 32,397.)
[19]
Sarkar, S.M.; Sultana, T.; Biswas, T.K.; Ranman, M.L.; Yusoff, M.M. New J. Chem. 2016, 40,497.
[20]
Liu, X.; Lin, B.; Zhang, Z.; Lei, H.; Li, Y. RSC Adv. 2016, 6,94399.
[21]
Jiang, Y.; Guo, N.; Li, X.; Sun, Y.; Zhang, W. Z. Naturforscher 2017, 72,549.
[22]
Martins, G.B. C.; Santos, M.R.; Rodrigues, M.V. R.; Sucupira, R.R.; Meneghetti, L.; Monteirob, A.L.; Suarez, P.A. Z. J. Braz. Chem. Soc. 2017, 28,2064.
[23]
Shojaei, S.; Ghasemi, Z.; Shahrisa, A. Appl. Organomet. Chem. 2017, 31,e3788.
[24]
Shojaei, S.; Ghasemi, Z.; Shahrisa, A. Tetrahedron Lett. 2017, 58,3957.
[25]
Maleki, A.; Eskandarpour, V.; Rahimi, J.; Hamidi, N. Carbohyd. Polym. 2019, 208,251.
[26]
Goswami, M.; Das, A.M. Carbohydr. Polym. 2018, 195,189.
[27]
Jeremic, S.; Djokic, L.; Runic, J.N. Int. J. Biol. Macromol. 2019, 129,351.
[28]
Sharpless, K.B. Angew. Chem. 2001, 113,2056.
[29]
Koga, H.; Azetsu, A.; Tokunaga, E.; Saito, T.; Isogaia, A.; Kitaoka, T. J. Mater. Chem. 2012, 22,5538.
[30]
Chavan, P.V.; Pandit, K.S.; Desai, U.V.; Kulkarnia, M.A.; Wadgaonkar, P.P. RSC Adv. 2014, 4,42137.
[31]
Pourjavadi, A.; Habibi, Z. RSC Adv. 2015, 5,99498.
[32]
Yu, W.; Jiang, L.; Shen, C.; Xu, W.; Zhang, P. Catal. Commun. 2016, 79,11.
[33]
Barrull, J.R.; Halluin, M.; Grognec, E.L.; F., X.; Felpin, E.L. Angew. Chem., Int. Ed. 2016, 55,1.
[34]
(a) Mandal, B.H.; Rahmanc, M.L.; Yusoffa, M.M.; Chonga, K.F.; Sarkar, S.M. Carbohydr. Polym. 2017, 156,175.
[34]
(b) Mandal, B.H.; Rahman, M.L.; Rahim, M.H. A.; Sarkar, S.M. ChemistrySelect 2016, 1,2750.
[35]
(a) Hajar, S.; Islam, M.S.; Sarkar, S.M. BioResources 2017, 12,882.
[35]
(b) Sarkar, S.M.; Rahman, M.L. J. Cleaner Prod. 2017, 141,683.
[35]
(c) Rahman, M.L.; Sarkar, S.M. J. Nanosci. Nanotechnol. 2017, 17,550.
[36]
Benhamou, K.; Kaddami, H.; Julve, M.; Stiriba, S. E. Biomacromolecules 2018, 7,200.
[37]
Sa?, D S.; Bustamante, R. A.; Rocha, C. E. R.; Silva, V. D.; Pandoli, O. G. ACS Sustainable Chem. Eng. 2019, 7,3267.
[38]
Hamzavi, S.F.; Gerivani, S.; Saeedi, S.; Naghdipari, K.; Shahverdizadeh, G. Mol. Diversity 2019, 24,201.
[39]
Baruah, D.; Saikia, U.P.; Pahari, P.; Konwar, D. Tetrahedron Lett. 2015, 56,2543.
[40]
Chauha, P.; Yan, N. RSC Adv. 2015, 5,37517.
[41]
Shaabani, A.; Hezarkhani, Z. Cellulose 2015, 22,3027.
[42]
Nekouei, F.; Nekouei, S.; Kargarzadeh, H. Chem. Eng. J. 2018, 335,567.
[43]
Dutta, A.; Chetia, M.; Ali, A.A.; Bordoloi, A.; Gehlot, P.S.; Kumar, A.; Sarma, D. Catal. Lett. 2019, 149,141.
[44]
Shim, S.W.; Noh, W.T.; Kwon, J.; Cho, J.Y.; Kim, K.S.; Kang, D.H. Bull. Korean Chem. Soc. 2002, 23,563.
[45]
Zhou, Z.; Lu, C.; Wu, X.; Zhang, X. RSC Adv. 2013, 3,26066.
[46]
Cheng, X.; Fu, A.; Li, H.; Wang, Y.; Guo, P.; Liu, J.; Zhang, J.; Zhao, X.S. ACS Sustainable Chem. Eng. 2015, 3,2414.
[47]
Khan, F.U.; Asimullah, Khan, S.B.; Kamal, T.; Asiri, A.M.; Khan, I.U.; Akhtar, K. Int. J. Biol. Macromol. 2017, 102,868.
[48]
Godiya, C.B.; Cheng, X.; Li, D.; Chen, Z.; Lu, X. J. Hazard. Mater. 2019, 364,28.
[49]
Ding, J.; Li, Q.; Xu, X.; Zhang, X.; Su, Y.; Yue, Q.; Gao, B. Carbohydr. Polym. 2018, 190,12.
[50]
Su, R.; Wang, F.; Ding, J.; Li, Q.; Zhou, W.; Liu, Y.; Gao, B.; Yue, Q. Carbohydr. Polym. 2019, 220,202.
[51]
Karami, S.; Zeynizadeh, B.; Shokri, Z. Cellulose 2018, 25,3295.
[52]
Karami, S.; Zeynizadeh, B. Carbohydr. Polym. 2019, 211,298.
[53]
Zhang, J.; Xie, W.; Liang, Q.; Peng, L.; He, L. ChemistrySelect 2019, 4,2846.
[54]
Lu, H.; Zhang, L.; Ma, J.; Alam, N.; Zhou, X.; Ni, Y. Nanomaterials 2019, 9,277.
[55]
Khan, S.A.; Khan, N.; Irum, U.; Farooq, A.; Asiri, A.M.; Bakhsh, E.M.; Khan, S.B. Int. J. Biol. Macromol. 2020, 153,806.
[56]
Hu, Y.; Li, G.; Y, Zhi.; Yao, Y.; Li, Z. China Synth. Fiber Ind. 2017, 40,24. (in Chinese)
[56]
( 胡英, 李国元, 颜志勇, 姚勇波, 李喆, 合成纤维工业, 2017, 40,24.)
[57]
Tavker, N.; Gaur, U.K.; Sharma, M. ACS Omega 2019, 4,11777.
[58]
Khalilzadeh, M.A.; Tajik, S.; Beitollahi, H.; Venditti, R.A. Ind. Eng. Chem. Res. 2020, 59,4219.
[59]
Zhou, Y.; Guo, X.; Li, X.; Fu, J.; Liu, J.; Hong, F.; Qiao, J. J. CO2 Util. 2020, 37,188.
[60]
Baruah, D.; Saikia, U. P.; Pahari, P.; Duttab, D.K.; Konwar, D. RSC Adv. 2014, 4,59338.
[61]
Baruah, D.; Konwar, D. Catal. Commun. 2015, 69,68.
[62]
Baruah, D.; Pahari, P.; Konwar, D. Tetrahedron Lett. 2015, 56,2543.
[63]
Darder, M.; Karan, A.; Real, G.; DeCoster, M.A. Mater. Sci. Eng., C 2020, 108,110369.
[64]
Sadanand, V.; Rajini, N.; Rajulu, A.V.; Satyanarayana, B. Carbohydr. Polym. 2016, 150,32.
[65]
El-Mossalamy, E.H.; Khalil, A.A.; Mohmoud, H.A. J. Basic Environ. Sci. 2018, 5,333.
[66]
Xu, Y.; Shi, Y.; Lei, F.; Dai, L. Carbohydr. Polym. 2020, 230,115671.
[67]
Ma, B.; Sun, B.; Huang, Y.; Chen, C.; Sun, D. Colloids Surf., A 2020, 590,124462.
Options
Outlines

/

〈 〉