Synthesis, characterization and catalytic performance of palladium supported on pyridine‐based covalent organic polymer for Suzuki‐Miyaura reaction
A bipyridine‐based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2′‐bipyridine‐5,5′‐diamine (Bpy) under ambient conditions. This material was modified by coordination of PdCl2 to COP framework, affording a hybrid material, Pd@TMC‐Bpy CO...
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| Published in | Applied organometallic chemistry Vol. 33; no. 10 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
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01.10.2019
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| Online Access | Get full text |
| ISSN | 0268-2605 1099-0739 |
| DOI | 10.1002/aoc.5172 |
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| Abstract | A bipyridine‐based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2′‐bipyridine‐5,5′‐diamine (Bpy) under ambient conditions. This material was modified by coordination of PdCl2 to COP framework, affording a hybrid material, Pd@TMC‐Bpy COP, which was applied as a highly efficient heterogeneous catalyst for Suzuki‐Miyaura reaction under ligand‐free conditions in ethyl lactate. The catalyst could be reused for five times without obvious loss of its activity.
A new covalent organic polymer immobilized Pd catalyst was synthesized and applied as a highly efficient heterogeneous catalyst for Suzuki‐Miyaura reaction under ligand‐free conditions in ethyl lactate. |
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| AbstractList | A bipyridine-based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2 '-bipyridine-5,5 '-diamine (Bpy) under ambient conditions. This material was modified by coordination of PdCl2 to COP framework, affording a hybrid material, Pd@TMC-Bpy COP, which was applied as a highly efficient heterogeneous catalyst for Suzuki-Miyaura reaction under ligand-free conditions in ethyl lactate. The catalyst could be reused for five times without obvious loss of its activity. A bipyridine‐based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2′‐bipyridine‐5,5′‐diamine (Bpy) under ambient conditions. This material was modified by coordination of PdCl2 to COP framework, affording a hybrid material, Pd@TMC‐Bpy COP, which was applied as a highly efficient heterogeneous catalyst for Suzuki‐Miyaura reaction under ligand‐free conditions in ethyl lactate. The catalyst could be reused for five times without obvious loss of its activity. A new covalent organic polymer immobilized Pd catalyst was synthesized and applied as a highly efficient heterogeneous catalyst for Suzuki‐Miyaura reaction under ligand‐free conditions in ethyl lactate. A bipyridine‐based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2′‐bipyridine‐5,5′‐diamine (Bpy) under ambient conditions. This material was modified by coordination of PdCl 2 to COP framework, affording a hybrid material, Pd@TMC‐Bpy COP, which was applied as a highly efficient heterogeneous catalyst for Suzuki‐Miyaura reaction under ligand‐free conditions in ethyl lactate. The catalyst could be reused for five times without obvious loss of its activity. |
| ArticleNumber | 5172 |
| Author | Han, Yi Zhao, Ai‐Dong Zhang, Zhan‐Hui Di, Jia‐Qi |
| Author_xml | – sequence: 1 givenname: Yi surname: Han fullname: Han, Yi organization: Hebei Normal University – sequence: 2 givenname: Jia‐Qi surname: Di fullname: Di, Jia‐Qi organization: Hebei Normal University – sequence: 3 givenname: Ai‐Dong surname: Zhao fullname: Zhao, Ai‐Dong email: aidongzhao@163.com organization: Hebei Normal University – sequence: 4 givenname: Zhan‐Hui orcidid: 0000-0002-1082-5773 surname: Zhang fullname: Zhang, Zhan‐Hui email: zhanhui@126.com organization: Hebei Normal University |
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| Cites_doi | 10.1002/slct.201702326 10.1016/j.carbpol.2016.03.019 10.1016/j.molstruc.2017.01.005 10.6023/cjoc201512014 10.1002/aoc.3888 10.1016/j.apcata.2017.11.018 10.1016/j.molstruc.2017.03.122 10.1039/C4PY01383B 10.1016/S1872-2067(15)61050-6 10.1016/j.jcis.2015.11.038 10.1021/acssuschemeng.7b02992 10.1002/cctc.201800400 10.1021/acs.chemmater.6b01370 10.1002/aoc.4102 10.1039/c3cs35521g 10.1039/C6GC00864J 10.1007/s10562-019-02739-1 10.1039/C6DT02242A 10.1002/chem.201701619 10.1002/adsc.201700671 10.1016/j.ijbiomac.2018.04.057 10.1002/cssc.200700159 10.1021/acsami.8b02080 10.1016/j.ultsonch.2018.03.017 10.1016/j.carbpol.2018.04.064 10.1016/j.apcata.2016.12.005 10.1039/C8GC02611D 10.1007/s10562-016-1851-1 10.1039/C5NJ02842F 10.1002/aoc.4846 10.6023/cjoc201711014 10.1002/chem.200401262 10.1039/C7CY00747G 10.1016/j.molcata.2015.06.008 10.1016/j.catcom.2016.09.028 10.1002/ajoc.201700680 10.1016/j.tet.2012.12.081 10.1002/aoc.4075 10.1039/C5CC02147B 10.1016/j.tet.2017.05.054 10.1016/j.molliq.2019.01.065 10.1021/acssuschemeng.7b01102 10.1016/j.molcata.2016.04.025 10.1002/slct.201801003 10.1016/j.molstruc.2016.05.091 10.1016/j.tet.2013.09.082 10.1016/j.apcata.2016.05.012 10.1016/j.jcis.2016.09.071 10.1002/aoc.4192 10.1016/j.jorganchem.2018.04.022 10.1002/adma.201505788 10.1016/j.molstruc.2018.01.074 10.1002/aoc.4346 10.1016/j.cej.2017.08.104 10.1016/j.apcata.2014.06.006 10.1021/acs.jpcc.7b07709 10.1021/acsami.8b07795 10.1016/j.jcis.2017.02.047 10.1021/acs.chemrev.7b00443 10.1002/cctc.201600774 10.1002/slct.201802977 10.1039/C7CP07686J 10.1007/s10562-019-02753-3 10.1080/10426507.2018.1542395 10.1016/j.carbpol.2016.06.103 10.1002/aoc.4076 10.1039/C5GC02264A 10.1002/aoc.3993 10.1016/j.molcata.2016.10.033 10.1016/j.apcata.2013.10.017 10.1039/C8TA11330K 10.1002/aoc.4632 10.1016/j.jorganchem.2017.10.011 10.1002/aoc.4594 10.1039/c7cy00747g 10.1039/c4py01383b 10.1039/c6dt02242a 10.1039/c5gc02264a 10.1039/c8gc02611d 10.1039/c8ta11330k 10.1039/c7cp07686j 10.1039/c5nj02842f 10.1039/c5cc02147b 10.1039/c6gc00864j |
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| Keywords | EFFICIENT HETEROGENEOUS CATALYST ONE-POT SYNTHESIS HIGHLY EFFICIENT heterogeneous catalyst DEEP EUTECTIC SOLVENT PD NANOPARTICLES PD(II) CATALYST GREEN SYNTHESIS RECYCLABLE CATALYST covalent organic polymer ethyl lactate MICROWAVE-ASSISTED SYNTHESIS C COUPLING REACTIONS Suzuki-Miyaura reaction |
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| References | 2018 2013; 118 42 2019; 7 2018; 122 2017; 7 2015; 6 2015; 51 2016 2017 2016; 8 853 45 2017; 23 2016; 465 2016; 146 2018 2018; 1160 866 2018 2019; 32 33 2018 2016 2016; 10 28 37 2018 2017 2017 2017 2014; 20 359 88 31 482 2008; 1 2018; 20 2018 2017 2016 2017 2019; 7 5 36 2 194 2018; 6 2019 2018 2013 2013; 278 38 69 69 2018; 550 2014; 469 2018; 3 2018; 195 2018 2018; 115 45 2017 2016; 531 523 2018 2018 2016 2017 2015 2016 2017 2016 2017; 32 32 145 496 407 420 1141 1122 1134 2016; 40 2016; 28 2017; 486 2018; 10 2018; 32 2005; 11 2016; 152 2016 2016 2018 2018 2019 2019 2019 2018 2017; 18 18 32 32 33 149 149 331 73 2017; 426 e_1_2_8_20_9 e_1_2_8_28_1 e_1_2_8_20_5 e_1_2_8_24_1 e_1_2_8_20_6 e_1_2_8_20_7 e_1_2_8_26_1 e_1_2_8_20_8 e_1_2_8_3_1 e_1_2_8_5_1 e_1_2_8_7_1 e_1_2_8_9_1 e_1_2_8_20_1 e_1_2_8_20_2 e_1_2_8_20_3 e_1_2_8_22_1 e_1_2_8_20_4 e_1_2_8_15_3 e_1_2_8_17_1 e_1_2_8_34_7 e_1_2_8_15_4 e_1_2_8_34_6 e_1_2_8_36_4 e_1_2_8_15_5 e_1_2_8_19_1 e_1_2_8_34_9 e_1_2_8_19_2 e_1_2_8_34_8 e_1_2_8_13_1 e_1_2_8_34_3 e_1_2_8_36_1 e_1_2_8_34_2 e_1_2_8_15_1 e_1_2_8_34_5 e_1_2_8_36_3 e_1_2_8_38_1 e_1_2_8_15_2 e_1_2_8_34_4 e_1_2_8_36_2 e_1_2_8_32_1 e_1_2_8_11_1 e_1_2_8_34_1 e_1_2_8_30_1 e_1_2_8_29_1 e_1_2_8_23_2 e_1_2_8_25_1 e_1_2_8_25_2 e_1_2_8_27_1 e_1_2_8_2_1 e_1_2_8_4_1 e_1_2_8_6_1 e_1_2_8_8_1 e_1_2_8_21_1 e_1_2_8_23_1 e_1_2_8_16_2 e_1_2_8_18_1 e_1_2_8_35_5 e_1_2_8_39_1 e_1_2_8_18_2 e_1_2_8_35_2 e_1_2_8_14_1 e_1_2_8_33_3 e_1_2_8_35_1 e_1_2_8_14_2 e_1_2_8_35_4 e_1_2_8_14_3 e_1_2_8_16_1 e_1_2_8_35_3 e_1_2_8_37_1 e_1_2_8_10_1 e_1_2_8_31_1 e_1_2_8_33_2 e_1_2_8_12_1 e_1_2_8_33_1 Sim, Y (WOS:000408079900015) 2017; 23 Baran, T (WOS:000428483500020) 2018; 1160 Khatioda, R (WOS:000435933100006) 2018; 3 Baran, T (WOS:000433204900006) 2018; 195 Sadhasivam, V (WOS:000443935100029) 2018; 10 Chen, W (WOS:000429280100050) 2018; 20 Gao, G (WOS:000434796800012) 2018; 38 Nasrollahzadeh, M (WOS:000367770100016) 2016; 465 Gao, G (WOS:000418400400031) 2017; 2 Adib, M (WOS:000378508900015) 2016; 40 Tadjarodi, A (WOS:000451408700025) 2018; 32 Baran, T (WOS:000381593700002) 2016; 523 Wang, HR (WOS:000431723400028) 2018; 10 Baran, T (WOS:000465575500006) 2019; 149 Baran, T (WOS:000394919100067) 2017; 1134 Guo, RY (WOS:000315062800014) 2013; 69 Baran, NY (WOS:000432600900011) 2018; 866 Baran, T (WOS:000423670000080) 2018; 32 Baran, T (WOS:000438662500029) 2018; 115 Khazaei, A (WOS:000411532100009) 2017; 73 Baran, T (WOS:000387097100021) 2017; 486 Ju, PY (WOS:000457893400025) 2019; 7 Heidari, B (WOS:000454321800054) 2019; 33 Elhage, A (WOS:000424728300026) 2018; 6 Baran, T (WOS:000375109200003) 2016; 145 Khatioda, R (WOS:000405806900023) 2017; 7 Zhang, M (WOS:000405139100063) 2017; 5 Baran, T (WOS:000465575500023) 2019; 149 Baran, T (WOS:000381167800013) 2016; 1122 Sharma, RK (WOS:000378178200002) 2016; 18 Wei, L (WOS:000376573700006) 2016; 36 Aiyappa, HB (WOS:000378973100031) 2016; 28 Roy, AS (WOS:000329266500039) 2014; 469 Biffis, A (WOS:000426614700017) 2018; 118 Tahmasebi, S (WOS:000417654800006) 2017; 853 Baran, NY (WOS:000392680500005) 2017; 531 Baran, T (WOS:000401593400061) 2017; 1141 Johnson, EM (WOS:000449887600017) 2018; 10 Baran, T (WOS:000378366300026) 2016; 420 Van Vaerenbergh, B (WOS:000423648900025) 2018; 550 Han, Y (WOS:000448822900011) 2018; 20 Augustyniak, AW (WOS:000382144300032) 2016; 45 Lichtenegger, GJ (WOS:000391076300006) 2017; 426 Arghan, M (WOS:000434047600013) 2018; 32 Xiang, ZH (WOS:000382479400015) 2016; 28 Baran, T (WOS:000361258900007) 2015; 407 Albrecht, M (WOS:000232081900026) 2005; 11 Gomes, R (WOS:000355985200033) 2015; 51 Sun, R (WOS:000386920700014) 2016; 8 Xiang, ZH (WOS:000350642400001) 2015; 6 Bahrami, K (WOS:000423670000094) 2018; 32 Mahdavi, H (WOS:000387325300009) 2016; 146 Kempasiddhaiah, M (WOS:000465346500016) 2019; 33 Baran, T (WOS:000432506900024) 2018; 45 Ma, CT (WOS:000419195800071) 2017; 31 Bhowmik, S (WOS:000422814200030) 2018; 122 Baran, T (WOS:000414155500013) 2018; 331 Zhang, JQ (WOS:000374082700002) 2016; 37 Baran, T (WOS:000380944500021) 2016; 152 Zhang, M (WOS:000389117500010) 2017; 88 Sadhasivam, V (WOS:000453917200020) 2018; 3 Mahanta, A (WOS:000426058000080) 2018; 32 Baran, T (WOS:000398425800048) 2017; 496 Gao, G (WOS:000473545900079) 2019; 194 Wan, JP (WOS:000425000600007) 2018; 7 Rathi, AK (WOS:000374413300014) 2016; 18 Guo, RY (WOS:000328010900002) 2013; 69 Dadras, A (WOS:000423670000002) 2018; 32 Han, FS (WOS:000319527400028) 2013; 42 Zhang, M (WOS:000413673600025) 2017; 359 Zhao, XN (WOS:000340306500031) 2014; 482 Schmoger, C (WOS:000256877000012) 2008; 1 Zhang, WH (WOS:000461526600015) 2019; 278 |
| References_xml | – volume: 6 start-page: 1717 year: 2018 publication-title: ACS Sustainable Chem. Eng. – volume: 3 year: 2018 publication-title: ChemistrySelect – volume: 195 start-page: 45 year: 2018 publication-title: Carbohydr. Polym. – volume: 32 start-page: e4192 year: 2018 publication-title: Appl. Organomet. Chem. – volume: 20 359 88 31 482 start-page: 4891 3618 39 258 year: 2018 2017 2017 2017 2014 publication-title: Green Chem. Adv. Synth. Catal. Catal. Commun. Appl. Organomet. Chem. Appl. Catal. A: Gen. – volume: 7 start-page: 3143 year: 2017 publication-title: Cat. Sci. Technol. – volume: 146 start-page: 2292 year: 2016 publication-title: Catal. Lett. – volume: 20 start-page: 6487 year: 2018 publication-title: Phys. Chem. Chem. Phys. – volume: 40 start-page: 4945 year: 2016 publication-title: New J. Chem. – volume: 122 start-page: 274 year: 2018 publication-title: J. Phys. Chem. C – volume: 550 start-page: 236 year: 2018 publication-title: Appl. Catal. A: Gen. – volume: 278 38 69 69 start-page: 124 846 2056 9931 year: 2019 2018 2013 2013 publication-title: J. Mol. Liq. Chin. J. Org. Chem. Tetrahedron Tetrahedron – volume: 1160 866 start-page: 154 87 year: 2018 2018 publication-title: J. Mol. Struct. J. Organomet. Chem. – volume: 32 year: 2018 publication-title: Appl. Organomet. Chem. – volume: 7 start-page: 2660 year: 2019 publication-title: J. Mater. Chem. A – volume: 51 year: 2015 publication-title: Chem. Commun. – volume: 115 45 start-page: 249 231 year: 2018 2018 publication-title: Int. J. Biol. Macromol. Ultrason. Sonochem. – volume: 32 33 start-page: e4632 year: 2018 2019 publication-title: Appl. Organomet. Chem. Appl. Organomet. Chem. – volume: 426 start-page: 39 year: 2017 publication-title: J. Mol. Catal. A: Chem. – volume: 11 start-page: 5742 year: 2005 publication-title: Chem. Eur. J. – volume: 23 year: 2017 publication-title: Chem. Eur. J. – volume: 10 start-page: 3833 year: 2018 publication-title: ChemCatChem – volume: 118 42 start-page: 2249 5270 year: 2018 2013 publication-title: Chem. Rev. Chem. Soc. Rev. – volume: 28 start-page: 6253 year: 2016 publication-title: Adv. Mater. – volume: 465 start-page: 121 year: 2016 publication-title: J. Colloid Interface Sci. – volume: 10 28 37 start-page: 4375 468 year: 2018 2016 2016 publication-title: ACS Appl. Mater. Interfaces Chem. Mater. Chin. J. Catal. – volume: 469 start-page: 320 year: 2014 publication-title: Appl. Catal. A: Gen. – volume: 152 start-page: 181 year: 2016 publication-title: Carbohydr. Polym. – volume: 1 start-page: 339 year: 2008 publication-title: ChemSusChem – volume: 6 start-page: 1896 year: 2015 publication-title: Polym. Chem. – volume: 3 start-page: 6309 year: 2018 publication-title: ChemistrySelect – volume: 7 5 36 2 194 start-page: 328 6175 954 11561 528 year: 2018 2017 2016 2017 2019 publication-title: Asian J. Org. Chem. ACS Sustainable Chem. Eng. Chin. J. Org. Chem. ChemistrySelect Phosphorus, Sulfur Silicon Relat. Elem. – volume: 32 32 145 496 407 420 1141 1122 1134 start-page: e4075 20 446 47 216 535 111 591 year: 2018 2018 2016 2017 2015 2016 2017 2016 2017 publication-title: Appl. Organomet. Chem. Appl. Organomet. Chem. Mentes, Carbohydr. Polym. J. Colloid Interface Sci. J. Mol. Catal. A: Chem. J. Mol. Catal. A: Chem. J. Mol. Struct. J. Mol. Struct. J. Mol. Struct. – volume: 18 18 32 32 33 149 149 331 73 start-page: 2363 3184 e4846 1496 1721 102 5624 year: 2016 2016 2018 2018 2019 2019 2019 2018 2017 publication-title: Green Chem. Green Chem. Appl. Organomet. Chem. Appl. Organomet. Chem. Appl. Organomet. Chem. Catal. Lett. Catal. Lett. Chem. Eng. J. Tetrahedron – volume: 531 523 start-page: 36 12 year: 2017 2016 publication-title: Appl. Catal. A: Gen. Appl. Catal. Gen. – volume: 10 year: 2018 publication-title: ACS Appl. Mater. Interfaces – volume: 486 start-page: 194 year: 2017 publication-title: J. Colloid Interface Sci. – volume: 8 853 45 start-page: 3261 35 year: 2016 2017 2016 publication-title: ChemCatChem J. Organomet. Chem. Dalton Trans. – ident: e_1_2_8_15_4 doi: 10.1002/slct.201702326 – ident: e_1_2_8_20_3 doi: 10.1016/j.carbpol.2016.03.019 – ident: e_1_2_8_20_9 doi: 10.1016/j.molstruc.2017.01.005 – ident: e_1_2_8_15_3 doi: 10.6023/cjoc201512014 – ident: e_1_2_8_35_4 doi: 10.1002/aoc.3888 – ident: e_1_2_8_29_1 doi: 10.1016/j.apcata.2017.11.018 – ident: e_1_2_8_20_7 doi: 10.1016/j.molstruc.2017.03.122 – ident: e_1_2_8_2_1 doi: 10.1039/C4PY01383B – ident: e_1_2_8_14_3 doi: 10.1016/S1872-2067(15)61050-6 – ident: e_1_2_8_26_1 doi: 10.1016/j.jcis.2015.11.038 – ident: e_1_2_8_32_1 doi: 10.1021/acssuschemeng.7b02992 – ident: e_1_2_8_11_1 doi: 10.1002/cctc.201800400 – ident: e_1_2_8_14_2 doi: 10.1021/acs.chemmater.6b01370 – ident: e_1_2_8_18_1 doi: 10.1002/aoc.4102 – ident: e_1_2_8_16_2 doi: 10.1039/c3cs35521g – ident: e_1_2_8_34_2 doi: 10.1039/C6GC00864J – ident: e_1_2_8_34_6 doi: 10.1007/s10562-019-02739-1 – ident: e_1_2_8_33_3 doi: 10.1039/C6DT02242A – ident: e_1_2_8_13_1 doi: 10.1002/chem.201701619 – ident: e_1_2_8_35_2 doi: 10.1002/adsc.201700671 – ident: e_1_2_8_23_1 doi: 10.1016/j.ijbiomac.2018.04.057 – ident: e_1_2_8_31_1 doi: 10.1002/cssc.200700159 – ident: e_1_2_8_4_1 doi: 10.1021/acsami.8b02080 – ident: e_1_2_8_23_2 doi: 10.1016/j.ultsonch.2018.03.017 – ident: e_1_2_8_21_1 doi: 10.1016/j.carbpol.2018.04.064 – ident: e_1_2_8_19_1 doi: 10.1016/j.apcata.2016.12.005 – ident: e_1_2_8_35_1 doi: 10.1039/C8GC02611D – ident: e_1_2_8_37_1 doi: 10.1007/s10562-016-1851-1 – ident: e_1_2_8_17_1 doi: 10.1039/C5NJ02842F – ident: e_1_2_8_34_5 doi: 10.1002/aoc.4846 – ident: e_1_2_8_36_2 doi: 10.6023/cjoc201711014 – ident: e_1_2_8_39_1 doi: 10.1002/chem.200401262 – ident: e_1_2_8_8_1 doi: 10.1039/C7CY00747G – ident: e_1_2_8_20_5 doi: 10.1016/j.molcata.2015.06.008 – ident: e_1_2_8_35_3 doi: 10.1016/j.catcom.2016.09.028 – ident: e_1_2_8_15_1 doi: 10.1002/ajoc.201700680 – ident: e_1_2_8_36_3 doi: 10.1016/j.tet.2012.12.081 – ident: e_1_2_8_20_1 doi: 10.1002/aoc.4075 – ident: e_1_2_8_7_1 doi: 10.1039/C5CC02147B – ident: e_1_2_8_34_9 doi: 10.1016/j.tet.2017.05.054 – ident: e_1_2_8_36_1 doi: 10.1016/j.molliq.2019.01.065 – ident: e_1_2_8_15_2 doi: 10.1021/acssuschemeng.7b01102 – ident: e_1_2_8_20_6 doi: 10.1016/j.molcata.2016.04.025 – ident: e_1_2_8_9_1 doi: 10.1002/slct.201801003 – ident: e_1_2_8_20_8 doi: 10.1016/j.molstruc.2016.05.091 – ident: e_1_2_8_36_4 doi: 10.1016/j.tet.2013.09.082 – ident: e_1_2_8_19_2 doi: 10.1016/j.apcata.2016.05.012 – ident: e_1_2_8_24_1 doi: 10.1016/j.jcis.2016.09.071 – ident: e_1_2_8_27_1 doi: 10.1002/aoc.4192 – ident: e_1_2_8_25_2 doi: 10.1016/j.jorganchem.2018.04.022 – ident: e_1_2_8_6_1 doi: 10.1002/adma.201505788 – ident: e_1_2_8_25_1 doi: 10.1016/j.molstruc.2018.01.074 – ident: e_1_2_8_34_3 doi: 10.1002/aoc.4346 – ident: e_1_2_8_34_8 doi: 10.1016/j.cej.2017.08.104 – ident: e_1_2_8_35_5 doi: 10.1016/j.apcata.2014.06.006 – ident: e_1_2_8_5_1 doi: 10.1021/acs.jpcc.7b07709 – ident: e_1_2_8_14_1 doi: 10.1021/acsami.8b07795 – ident: e_1_2_8_20_4 doi: 10.1016/j.jcis.2017.02.047 – ident: e_1_2_8_16_1 doi: 10.1021/acs.chemrev.7b00443 – ident: e_1_2_8_33_1 doi: 10.1002/cctc.201600774 – ident: e_1_2_8_10_1 doi: 10.1002/slct.201802977 – ident: e_1_2_8_3_1 doi: 10.1039/C7CP07686J – ident: e_1_2_8_34_7 doi: 10.1007/s10562-019-02753-3 – ident: e_1_2_8_15_5 doi: 10.1080/10426507.2018.1542395 – ident: e_1_2_8_22_1 doi: 10.1016/j.carbpol.2016.06.103 – ident: e_1_2_8_20_2 doi: 10.1002/aoc.4076 – ident: e_1_2_8_34_1 doi: 10.1039/C5GC02264A – ident: e_1_2_8_34_4 doi: 10.1002/aoc.3993 – ident: e_1_2_8_30_1 doi: 10.1016/j.molcata.2016.10.033 – ident: e_1_2_8_38_1 doi: 10.1016/j.apcata.2013.10.017 – ident: e_1_2_8_12_1 doi: 10.1039/C8TA11330K – ident: e_1_2_8_18_2 doi: 10.1002/aoc.4632 – ident: e_1_2_8_33_2 doi: 10.1016/j.jorganchem.2017.10.011 – ident: e_1_2_8_28_1 doi: 10.1002/aoc.4594 – volume: 482 start-page: 258 year: 2014 ident: WOS:000340306500031 article-title: Magnetic CoFe2O4 nanoparticle immobilized N-propyl diethylenetriamine sulfamic acid as an efficient and recyclable catalyst for the synthesis of amides via the Ritter reaction publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2014.06.006 – volume: 3 start-page: 6309 year: 2018 ident: WOS:000435933100006 article-title: Cu(II) Complex onto a Pyridine-Based Porous Organic Polymer as a Heterogeneous Catalyst for Nitroarene Reduction publication-title: CHEMISTRYSELECT doi: 10.1002/slct.201801003 – volume: 146 start-page: 2292 year: 2016 ident: WOS:000387325300009 article-title: Polyacrylamide-g-Reduced Graphene Oxide Supported Pd Nanoparticles as a Highly Efficient Catalyst for Suzuki-Miyaura Reactions in Water publication-title: CATALYSIS LETTERS doi: 10.1007/s10562-016-1851-1 – volume: 45 start-page: 231 year: 2018 ident: WOS:000432506900024 article-title: Ultrasound-accelerated synthesis of biphenyl compounds using novel Pd(0) nanoparticles immobilized on bio-composite publication-title: ULTRASONICS SONOCHEMISTRY doi: 10.1016/j.ultsonch.2018.03.017 – volume: 69 start-page: 2056 year: 2013 ident: WOS:000315062800014 article-title: One-pot three-component synthesis of functionalized spirooxindoles in gluconic acid aqueous solution publication-title: TETRAHEDRON doi: 10.1016/j.tet.2012.12.081 – volume: 7 start-page: 3143 year: 2017 ident: WOS:000405806900023 article-title: Constructing two dimensional amide porous polymer to promote selective oxidation reactions publication-title: CATALYSIS SCIENCE & TECHNOLOGY doi: 10.1039/c7cy00747g – volume: 486 start-page: 194 year: 2017 ident: WOS:000387097100021 article-title: Design and application of sporopollenin microcapsule supported palladium catalyst: Remarkably high turnover frequency and reusability in catalysis of biaryls publication-title: JOURNAL OF COLLOID AND INTERFACE SCIENCE doi: 10.1016/j.jcis.2016.09.071 – volume: 122 start-page: 274 year: 2018 ident: WOS:000422814200030 article-title: Nanoporous Conducting Covalent Organic Polymer (COP) Nanostructures as Metal-Free High Performance Visible-Light Photocatalyst for Water Treatment and Enhanced CO2 Capture publication-title: JOURNAL OF PHYSICAL CHEMISTRY C doi: 10.1021/acs.jpcc.7b07709 – volume: 32 start-page: ARTN e4192 year: 2018 ident: WOS:000426058000080 article-title: Methanol aided synthesis of PdNPs decorated on montmorillonite K 10 and its implication in Suzuki Miyaura type cross coupling reaction under base free condition publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4192 – volume: 149 start-page: 1496 year: 2019 ident: WOS:000465575500006 article-title: Production and Application of Highly Efficient and Reusable Palladium Nanocatalyst Decorated on the Magnetically Retrievable Chitosan/Activated Carbon Composite Microcapsules publication-title: CATALYSIS LETTERS doi: 10.1007/s10562-019-02739-1 – volume: 33 start-page: ARTN e4846 year: 2019 ident: WOS:000465346500016 article-title: Magnetite tethered mesoionic carbene-palladium (II): An efficient and reusable nanomagnetic catalyst for Suzuki-Miyaura and Mizoroki-Heck cross-coupling reactions in aqueous medium publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4846 – volume: 6 start-page: 1896 year: 2015 ident: WOS:000350642400001 article-title: Well-defined two dimensional covalent organic polymers: rational design, controlled syntheses, and potential applications publication-title: POLYMER CHEMISTRY doi: 10.1039/c4py01383b – volume: 37 start-page: 468 year: 2016 ident: WOS:000374082700002 article-title: Nitrogen ligands in two-dimensional covalent organic frameworks for metal catalysis publication-title: CHINESE JOURNAL OF CATALYSIS doi: 10.1016/S1872-2067(15)61050-6 – volume: 10 start-page: 37919 year: 2018 ident: WOS:000449887600017 article-title: Covalent-Organic Frameworks Composed of Rhenium Bipyridine and Metal Porphyrins: Designing Heterobimetallic Frameworks with Two Distinct Metal Sites publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.8b07795 – volume: 531 start-page: 36 year: 2017 ident: WOS:000392680500005 article-title: Fabrication and application of cellulose Schiff base supported Pd(II) catalyst for fast and simple synthesis of biaryls via Suzuki coupling reaction publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2016.12.005 – volume: 45 start-page: 13525 year: 2016 ident: WOS:000382144300032 article-title: Palladium nanoparticles supported on a nickel pyrazolate metal organic framework as a catalyst for Suzuki and carbonylative Suzuki couplings publication-title: DALTON TRANSACTIONS doi: 10.1039/c6dt02242a – volume: 550 start-page: 236 year: 2018 ident: WOS:000423648900025 article-title: The effect of the hydrotalcite structure and nanoparticle size on the catalytic performance of supported palladium nanoparticle catalysts in Suzuki cross-coupling publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2017.11.018 – volume: 32 start-page: ARTN e4102 year: 2018 ident: WOS:000423670000094 article-title: Synthesis, characterization and application of graphene palladium porphyrin as a nanocatalyst for the coupling reactions such as: Suzuki-Miyaura and Mizoroki-Heck publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4102 – volume: 194 start-page: 528 year: 2019 ident: WOS:000473545900079 article-title: Catalyst free one-pot synthesis of -aminophosphonates in aqueous ethyl lactate publication-title: PHOSPHORUS SULFUR AND SILICON AND THE RELATED ELEMENTS doi: 10.1080/10426507.2018.1542395 – volume: 88 start-page: 39 year: 2017 ident: WOS:000389117500010 article-title: Supported molybdenum on graphene oxide/Fe3O4: An efficient, magnetically separable catalyst for one-pot construction of spiro-oxindole dihydropyridines in deep eutectic solvent under microwave irradiation publication-title: CATALYSIS COMMUNICATIONS doi: 10.1016/j.catcom.2016.09.028 – volume: 5 start-page: 6175 year: 2017 ident: WOS:000405139100063 article-title: Catalyst-Free, Visible-Light Promoted One-Pot Synthesis of Spirooxindole-Pyran Derivatives in Aqueous Ethyl Lactate publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/acssuschemeng.7b01102 – volume: 18 start-page: 2363 year: 2016 ident: WOS:000374413300014 article-title: Maghemite decorated with ultra-small palladium nanoparticles (gamma-Fe2O3-Pd): applications in the Heck-Mizoroki olefination, Suzuki reaction and allylic oxidation of alkenes publication-title: GREEN CHEMISTRY doi: 10.1039/c5gc02264a – volume: 149 start-page: 1721 year: 2019 ident: WOS:000465575500023 article-title: Biosynthesis of Highly Retrievable Magnetic Palladium Nanoparticles Stabilized on Bio-composite for Production of Various Biaryl Compounds and Catalytic Reduction of 4-Nitrophenol publication-title: CATALYSIS LETTERS doi: 10.1007/s10562-019-02753-3 – volume: 10 start-page: 3833 year: 2018 ident: WOS:000443935100029 article-title: Palladium Nanoparticles Supported on Nitrogen-rich Containing Melamine-based Microporous Covalent Triazine Polymers as Efficient Heterogeneous Catalyst for C-Se Coupling Reactions publication-title: CHEMCATCHEM doi: 10.1002/cctc.201800400 – volume: 195 start-page: 45 year: 2018 ident: WOS:000433204900006 article-title: Pd(0) nanocatalyst stabilized on a novel agar/pectin composite and its catalytic activity in the synthesis of biphenyl compounds by Suzuki-Miyaura cross coupling reaction and reduction of o-nitroaniline publication-title: CARBOHYDRATE POLYMERS doi: 10.1016/j.carbpol.2018.04.064 – volume: 1134 start-page: 591 year: 2017 ident: WOS:000394919100067 article-title: Construction of new biopolymer (chitosan)-based pincer-type Pd(II) complex and its catalytic application in Suzuki cross coupling reactions publication-title: JOURNAL OF MOLECULAR STRUCTURE doi: 10.1016/j.molstruc.2017.01.005 – volume: 1 start-page: 339 year: 2008 ident: WOS:000256877000012 article-title: Pd on porous glass: A versatile and easily recyclable catalyst for Suzuki and Heck reactions publication-title: CHEMSUSCHEM doi: 10.1002/cssc.200700159 – volume: 278 start-page: 124 year: 2019 ident: WOS:000461526600015 article-title: Choline chloride and lactic acid: A natural deep eutectic solvent for one-pot rapid construction of spiro[indoline-3,4 '-pyrazolo[3,4-b]pyridines] publication-title: JOURNAL OF MOLECULAR LIQUIDS doi: 10.1016/j.molliq.2019.01.065 – volume: 426 start-page: 39 year: 2017 ident: WOS:000391076300006 article-title: Suzuki-Miyaura coupling reactions using novel metal oxide supported ionic palladium catalysts publication-title: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL doi: 10.1016/j.molcata.2016.10.033 – volume: 118 start-page: 2249 year: 2018 ident: WOS:000426614700017 article-title: Pd Metal Catalysts for Cross-Couplings and Related Reactions in the 21st Century: A Critical Review publication-title: CHEMICAL REVIEWS doi: 10.1021/acs.chemrev.7b00443 – volume: 20 start-page: 4891 year: 2018 ident: WOS:000448822900011 article-title: Copper immobilized at a covalent organic framework: an efficient and recyclable heterogeneous catalyst for the Chan-Lam coupling reaction of aryl boronic acids and amines publication-title: GREEN CHEMISTRY doi: 10.1039/c8gc02611d – volume: 38 start-page: 846 year: 2018 ident: WOS:000434796800012 article-title: Deep Eutectic Solvent Catalyzed One-Pot Synthesis of 4,7-Dihydro-1H-pyrazolo[3,4-b]pyridine-5-carbonitriles publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201711014 – volume: 145 start-page: 20 year: 2016 ident: WOS:000375109200003 article-title: Synthesis, characterization, and catalytic activity in Suzuki coupling and catalase-like reactions of new chitosan supported Pd catalyst publication-title: CARBOHYDRATE POLYMERS doi: 10.1016/j.carbpol.2016.03.019 – volume: 6 start-page: 1717 year: 2018 ident: WOS:000424728300026 article-title: Light-Induced Sonogashira C-C Coupling under Mild Conditions Using Supported Palladium Nanoparticles publication-title: ACS SUSTAINABLE CHEMISTRY & ENGINEERING doi: 10.1021/acssuschemeng.7b02992 – volume: 469 start-page: 320 year: 2014 ident: WOS:000329266500039 article-title: Pd-grafted porous metal-organic framework material as an efficient and reusable heterogeneous catalyst for C-C coupling reactions in water publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2013.10.017 – volume: 7 start-page: 2660 year: 2019 ident: WOS:000457893400025 article-title: Salen-porphyrin-based conjugated microporous polymer supported Pd nanoparticles: highly efficient heterogeneous catalysts for aqueous C-C coupling reactions publication-title: JOURNAL OF MATERIALS CHEMISTRY A doi: 10.1039/c8ta11330k – volume: 420 start-page: 216 year: 2016 ident: WOS:000378366300026 article-title: An environmental catalyst derived from biological waste materials for green synthesis of biaryls via Suzuki coupling reactions publication-title: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL doi: 10.1016/j.molcata.2016.04.025 – volume: 11 start-page: 5742 year: 2005 ident: WOS:000232081900026 article-title: 5,5 '-diamino-2,2 '-bipyridine: A versatile building block for the synthesis of bipyridine/catechol ligands that form homo- and heteronuclear helicates publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.200401262 – volume: 7 start-page: 328 year: 2018 ident: WOS:000425000600007 article-title: Iodine-Catalyzed, Ethyl-Lactate-Mediated Synthesis of 1,4-Benzothiazines via Metal-Free Cascade Enaminone Transamination and C-H Sulfenylation publication-title: ASIAN JOURNAL OF ORGANIC CHEMISTRY doi: 10.1002/ajoc.201700680 – volume: 523 start-page: 12 year: 2016 ident: WOS:000381593700002 article-title: Exceptionally high turnover frequencies recorded for a new chitosan-based palladium(II) catalyst publication-title: APPLIED CATALYSIS A-GENERAL doi: 10.1016/j.apcata.2016.05.012 – volume: 36 start-page: 954 year: 2016 ident: WOS:000376573700006 article-title: Recent Advances in Organic Synthesis Employing Ethyl Lactate as Green Reaction Medium publication-title: CHINESE JOURNAL OF ORGANIC CHEMISTRY doi: 10.6023/cjoc201512014 – volume: 3 start-page: 13442 year: 2018 ident: WOS:000453917200020 article-title: Porous Triazine Containing Covalent Organic Polymer Supported Pd Nanoparticles: A Stable and Efficient Heterogeneous Catalyst for Sonogashira Cross-Coupling and the Reduction of Nitroarenes publication-title: CHEMISTRYSELECT doi: 10.1002/slct.201802977 – volume: 69 start-page: 9931 year: 2013 ident: WOS:000328010900002 article-title: Meglumine promoted one-pot, four-component synthesis of pyranopyrazole derivatives publication-title: TETRAHEDRON doi: 10.1016/j.tet.2013.09.082 – volume: 23 start-page: 11279 year: 2017 ident: WOS:000408079900015 article-title: Mechanochemical Synthesis of Phosphazane-Based Frameworks publication-title: CHEMISTRY-A EUROPEAN JOURNAL doi: 10.1002/chem.201701619 – volume: 20 start-page: 6487 year: 2018 ident: WOS:000429280100050 article-title: Lithium doping on 2D squaraine-bridged covalent organic polymers for enhancing adsorption properties: a theoretical study publication-title: PHYSICAL CHEMISTRY CHEMICAL PHYSICS doi: 10.1039/c7cp07686j – volume: 40 start-page: 4945 year: 2016 ident: WOS:000378508900015 article-title: Palladium NPs supported on novel imin-opyridine-functionalized MWCNTs: efficient and highly reusable catalysts for the Suzuki-Miyaura and Sonogashira coupling reactions publication-title: NEW JOURNAL OF CHEMISTRY doi: 10.1039/c5nj02842f – volume: 32 start-page: ARTN e4594 year: 2018 ident: WOS:000451408700025 article-title: Green synthesis and characterization of palladium nanoparticles supported on zeolite Y by sonochemical method, powerful and efficient catalyst for Suzuki-Miyaura coupling of aryl halides with phenylboronic acid publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4594 – volume: 32 start-page: ARTN e4346 year: 2018 ident: WOS:000434047600013 article-title: Mizoroki-Heck and Suzuki-Miyaura reactions mediated by poly(2-acrylamido-2-methyl-1-propanesulfonic acid)-stabilized magnetically separable palladium catalyst publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4346 – volume: 853 start-page: 35 year: 2017 ident: WOS:000417654800006 article-title: One-step synthesis of Pd-NPs@Cu-2(BDC)(2)DABCO as efficient heterogeneous catalyst for the Suzuki-Miyaura cross-coupling reaction publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY doi: 10.1016/j.jorganchem.2017.10.011 – volume: 31 start-page: ARTN e3888 year: 2017 ident: WOS:000419195800071 article-title: Magnetic copper ferrite catalyzed homo- and cross-coupling reaction of terminal alkynes under ambient atmosphere publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.3888 – volume: 152 start-page: 181 year: 2016 ident: WOS:000380944500021 article-title: Green heterogeneous Pd(II) catalyst produced from chitosan-cellulose micro beads for green synthesis of biaryls publication-title: CARBOHYDRATE POLYMERS doi: 10.1016/j.carbpol.2016.06.103 – volume: 33 start-page: ARTN e4632 year: 2019 ident: WOS:000454321800054 article-title: Novel palladium nanoparticles supported on beta-cyclodextrin@graphene oxide as magnetically recyclable catalyst for Suzuki-Miyaura cross-coupling reaction with two different approaches in bio-based solvents publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4632 – volume: 465 start-page: 121 year: 2016 ident: WOS:000367770100016 article-title: Green synthesis, characterization and catalytic activity of the Pd/TiO2 nanoparticles for the ligand-free Suzuki-Miyaura coupling reaction publication-title: JOURNAL OF COLLOID AND INTERFACE SCIENCE doi: 10.1016/j.jcis.2015.11.038 – volume: 8 start-page: 3261 year: 2016 ident: WOS:000386920700014 article-title: Palladium(II)@Zirconium-Based Mixed-Linker Metal-Organic Frameworks as Highly Efficient and Recyclable Catalysts for Suzuki and Heck Cross-Coupling Reactions publication-title: CHEMCATCHEM doi: 10.1002/cctc.201600774 – volume: 32 start-page: ARTN e4075 year: 2018 ident: WOS:000423670000080 article-title: Sustainable chitosan/starch composite material for stabilization of palladium nanoparticles: Synthesis, characterization and investigation of catalytic behaviour of Pd@chitosan/starch nanocomposite in Suzuki-Miyaura reaction publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.4075 – volume: 115 start-page: 249 year: 2018 ident: WOS:000438662500029 article-title: An easily recoverable and highly reproducible agar-supported palladium catalyst for Suzuki-Miyaura coupling reactions and reduction of o-nitroaniline publication-title: INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES doi: 10.1016/j.ijbiomac.2018.04.057 – volume: 496 start-page: 446 year: 2017 ident: WOS:000398425800048 article-title: Practical, economical, and eco-friendly starch -supported palladium catalyst for Suzuki coupling reactions publication-title: JOURNAL OF COLLOID AND INTERFACE SCIENCE doi: 10.1016/j.jcis.2017.02.047 – volume: 1122 start-page: 111 year: 2016 ident: WOS:000381167800013 article-title: Microwave assisted synthesis of biarlys by C-C coupling reactions with a new chitosan supported Pd(II) catalyst publication-title: JOURNAL OF MOLECULAR STRUCTURE doi: 10.1016/j.molstruc.2016.05.091 – volume: 1141 start-page: 535 year: 2017 ident: WOS:000401593400061 article-title: A new chitosan Schiff base supported Pd(II) complex for microwave-assisted synthesis of biaryls compounds publication-title: JOURNAL OF MOLECULAR STRUCTURE doi: 10.1016/j.molstruc.2017.03.122 – volume: 73 start-page: 5624 year: 2017 ident: WOS:000411532100009 article-title: Nano-Fe3O4@SiO2 supported Pd(0) as a magnetically recoverable nanocatalyst for Suzuki coupling reaction in the presence of waste eggshell as low-cost natural base publication-title: TETRAHEDRON doi: 10.1016/j.tet.2017.05.054 – volume: 407 start-page: 47 year: 2015 ident: WOS:000361258900007 article-title: Carboxymethyl chitosan Schiff base supported heterogeneous palladium(II) catalysts for Suzuki cross-coupling reaction publication-title: JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL doi: 10.1016/j.molcata.2015.06.008 – volume: 51 start-page: 10050 year: 2015 ident: WOS:000355985200033 article-title: A triazine-based covalent organic polymer for efficient CO2 adsorption publication-title: CHEMICAL COMMUNICATIONS doi: 10.1039/c5cc02147b – volume: 359 start-page: 3618 year: 2017 ident: WOS:000413673600025 article-title: A General and Practical Approach for the Synthesis of 1,2,4-Trioxanes Catalyzed by Silica-Ferric Chloride publication-title: ADVANCED SYNTHESIS & CATALYSIS doi: 10.1002/adsc.201700671 – volume: 28 start-page: 4375 year: 2016 ident: WOS:000378973100031 article-title: Cobalt-Modified Covalent Organic Framework as a Robust Water Oxidation Electrocatalyst publication-title: CHEMISTRY OF MATERIALS doi: 10.1021/acs.chemmater.6b01370 – volume: 18 start-page: 3184 year: 2016 ident: WOS:000378178200002 article-title: Fe3O4 (iron oxide)-supported nanocatalysts: synthesis, characterization and applications in coupling reactions publication-title: GREEN CHEMISTRY doi: 10.1039/c6gc00864j – volume: 1160 start-page: 154 year: 2018 ident: WOS:000428483500020 article-title: Preparation, structural characterization, and catalytic performance of Pd(II) and Pt(II) complexes derived from cellulose Schiff base publication-title: JOURNAL OF MOLECULAR STRUCTURE doi: 10.1016/j.molstruc.2018.01.074 – volume: 2 start-page: 11561 year: 2017 ident: WOS:000418400400031 article-title: Catalyst Free Synthesis of Bis(Indolyl)Methanes and 3,3-Bis(Indolyl)oxindoles in Aqueous Ethyl Lactate publication-title: CHEMISTRYSELECT doi: 10.1002/slct.201702326 – volume: 331 start-page: 102 year: 2018 ident: WOS:000414155500013 article-title: Production of magnetically recoverable, thermally stable, bio-based catalyst: Remarkable turnover frequency and reusability in Suzuki coupling reaction publication-title: CHEMICAL ENGINEERING JOURNAL doi: 10.1016/j.cej.2017.08.104 – volume: 32 start-page: ARTN e3993 year: 2018 ident: WOS:000423670000002 article-title: Suzuki-Miyaura coupling reaction in water in the presence of robust palladium immobilized on modified magnetic Fe3O4 nanoparticles as a recoverable catalyst publication-title: APPLIED ORGANOMETALLIC CHEMISTRY doi: 10.1002/aoc.3993 – volume: 42 start-page: 5270 year: 2013 ident: WOS:000319527400028 article-title: Transition-metal-catalyzed Suzuki-Miyaura cross-coupling reactions: a remarkable advance from palladium to nickel catalysts publication-title: CHEMICAL SOCIETY REVIEWS doi: 10.1039/c3cs35521g – volume: 866 start-page: 87 year: 2018 ident: WOS:000432600900011 article-title: Highly effective and recoverable Pd(II) catalyst immobilized on thermally stable Schiff base polymer containing phenol group: Production, characterization and application in Suzuki coupling reactions publication-title: JOURNAL OF ORGANOMETALLIC CHEMISTRY doi: 10.1016/j.jorganchem.2018.04.022 – volume: 28 start-page: 6253 year: 2016 ident: WOS:000382479400015 article-title: Edge Functionalization of Graphene and Two-Dimensional Covalent Organic Polymers for Energy Conversion and Storage publication-title: ADVANCED MATERIALS doi: 10.1002/adma.201505788 – volume: 10 start-page: 14475 year: 2018 ident: WOS:000431723400028 article-title: pH-Responsive Nanoscale Covalent Organic Polymers as a Biodegradable Drug Carrier for Combined Photodynamic Chemotherapy of Cancer publication-title: ACS APPLIED MATERIALS & INTERFACES doi: 10.1021/acsami.8b02080 |
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| Snippet | A bipyridine‐based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2′‐bipyridine‐5,5′‐diamine... A bipyridine-based covalent organic polymer (COP) was successfully synthesized by condensation of trimesoyl chloride (TMC) and 2,2 '-bipyridine-5,5 '-diamine... |
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| SubjectTerms | Catalysis Catalysts Chemical synthesis Chemistry Chemistry, Applied Chemistry, Inorganic & Nuclear Condensates Condensation polymerization covalent organic polymer Ethyl lactate heterogeneous catalyst Palladium Physical Sciences Polymers Science & Technology Suzuki‐Miyaura reaction |
| Title | Synthesis, characterization and catalytic performance of palladium supported on pyridine‐based covalent organic polymer for Suzuki‐Miyaura reaction |
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