Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactideElectronic supplementary information (ESI) available. CCDC 1880806-1880809. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt04938f
Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl 2 (TMG4NMe 2 asme)], [ZnCl 2 (TMG5Clasme)], [ZnCl 2 (TMG5Measme)] and [ZnCl 2 (TMG5NMe 2 asme)] with...
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creator | Schäfer, Pascal M McKeown, Paul Fuchs, Martin Rittinghaus, Ruth D Hermann, Alina Henkel, Johanna Seidel, Sebastian Roitzheim, Christoph Ksiazkiewicz, Agnieszka N Hoffmann, Alexander Pich, Andrij Jones, Matthew D Herres-Pawlis, Sonja |
description | Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl
2
(TMG4NMe
2
asme)], [ZnCl
2
(TMG5Clasme)], [ZnCl
2
(TMG5Measme)] and [ZnCl
2
(TMG5NMe
2
asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of
rac
-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl
2
(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the
para
-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the
meta
-position causes no change in the reaction rate. With molecular weights over 71 000 g mol
−1
being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)
2
. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.
Four non-toxic, highly active and robust complexes have been used in the ring opening polymerisation of non-purifed lactide to substitute Sn(Oct)
2
. |
doi_str_mv | 10.1039/c8dt04938f |
format | Article |
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2
(TMG4NMe
2
asme)], [ZnCl
2
(TMG5Clasme)], [ZnCl
2
(TMG5Measme)] and [ZnCl
2
(TMG5NMe
2
asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of
rac
-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl
2
(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the
para
-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the
meta
-position causes no change in the reaction rate. With molecular weights over 71 000 g mol
−1
being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)
2
. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.
Four non-toxic, highly active and robust complexes have been used in the ring opening polymerisation of non-purifed lactide to substitute Sn(Oct)
2
.</description><identifier>ISSN: 1477-9226</identifier><identifier>EISSN: 1477-9234</identifier><identifier>DOI: 10.1039/c8dt04938f</identifier><language>eng</language><creationdate>2019-05</creationdate><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids></links><search><creatorcontrib>Schäfer, Pascal M</creatorcontrib><creatorcontrib>McKeown, Paul</creatorcontrib><creatorcontrib>Fuchs, Martin</creatorcontrib><creatorcontrib>Rittinghaus, Ruth D</creatorcontrib><creatorcontrib>Hermann, Alina</creatorcontrib><creatorcontrib>Henkel, Johanna</creatorcontrib><creatorcontrib>Seidel, Sebastian</creatorcontrib><creatorcontrib>Roitzheim, Christoph</creatorcontrib><creatorcontrib>Ksiazkiewicz, Agnieszka N</creatorcontrib><creatorcontrib>Hoffmann, Alexander</creatorcontrib><creatorcontrib>Pich, Andrij</creatorcontrib><creatorcontrib>Jones, Matthew D</creatorcontrib><creatorcontrib>Herres-Pawlis, Sonja</creatorcontrib><title>Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactideElectronic supplementary information (ESI) available. CCDC 1880806-1880809. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt04938f</title><description>Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl
2
(TMG4NMe
2
asme)], [ZnCl
2
(TMG5Clasme)], [ZnCl
2
(TMG5Measme)] and [ZnCl
2
(TMG5NMe
2
asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of
rac
-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl
2
(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the
para
-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the
meta
-position causes no change in the reaction rate. With molecular weights over 71 000 g mol
−1
being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)
2
. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.
Four non-toxic, highly active and robust complexes have been used in the ring opening polymerisation of non-purifed lactide to substitute Sn(Oct)
2
.</description><issn>1477-9226</issn><issn>1477-9234</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2019</creationdate><recordtype>article</recordtype><sourceid/><recordid>eNqFkM1Lw0AQxRdRsH5cvAvPm4Ktm6S2Sa9pi71Y0d7LdLNpVzabsLsp1D_cswsVexD09Abem_k9hrGriPcinmQPIi0872dJWh6xTtQfDrtZnPSPf-Z4cMrOnHvnPI75Y9xhn4vWKLMGwdar1nm4nfOyGuH5fo4PZQTWLRlVKCMhyJMOtkNZW_iNxOv8BXUJTcKrQk60FN7WRgm4tmm0rKTxZHdQJixU5FVtcDt5m92BtqQ0rbTsIc_HOaI05SkfdPea9TANhJAEmQLCBihpXa8tNZtwvQhFwlHksylCrg5VLOSBvqfBSYnxfDbC7-9csJOStJOX33rOrqeTRf7UtU4sG6uqUHt5iCf_-zd_-cumKJMvEAaCIw</recordid><startdate>20190507</startdate><enddate>20190507</enddate><creator>Schäfer, Pascal M</creator><creator>McKeown, Paul</creator><creator>Fuchs, Martin</creator><creator>Rittinghaus, Ruth D</creator><creator>Hermann, Alina</creator><creator>Henkel, Johanna</creator><creator>Seidel, Sebastian</creator><creator>Roitzheim, Christoph</creator><creator>Ksiazkiewicz, Agnieszka N</creator><creator>Hoffmann, Alexander</creator><creator>Pich, Andrij</creator><creator>Jones, Matthew D</creator><creator>Herres-Pawlis, Sonja</creator><scope/></search><sort><creationdate>20190507</creationdate><title>Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactideElectronic supplementary information (ESI) available. CCDC 1880806-1880809. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt04938f</title><author>Schäfer, Pascal M ; McKeown, Paul ; Fuchs, Martin ; Rittinghaus, Ruth D ; Hermann, Alina ; Henkel, Johanna ; Seidel, Sebastian ; Roitzheim, Christoph ; Ksiazkiewicz, Agnieszka N ; Hoffmann, Alexander ; Pich, Andrij ; Jones, Matthew D ; Herres-Pawlis, Sonja</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-rsc_primary_c8dt04938f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2019</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Schäfer, Pascal M</creatorcontrib><creatorcontrib>McKeown, Paul</creatorcontrib><creatorcontrib>Fuchs, Martin</creatorcontrib><creatorcontrib>Rittinghaus, Ruth D</creatorcontrib><creatorcontrib>Hermann, Alina</creatorcontrib><creatorcontrib>Henkel, Johanna</creatorcontrib><creatorcontrib>Seidel, Sebastian</creatorcontrib><creatorcontrib>Roitzheim, Christoph</creatorcontrib><creatorcontrib>Ksiazkiewicz, Agnieszka N</creatorcontrib><creatorcontrib>Hoffmann, Alexander</creatorcontrib><creatorcontrib>Pich, Andrij</creatorcontrib><creatorcontrib>Jones, Matthew D</creatorcontrib><creatorcontrib>Herres-Pawlis, Sonja</creatorcontrib></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Schäfer, Pascal M</au><au>McKeown, Paul</au><au>Fuchs, Martin</au><au>Rittinghaus, Ruth D</au><au>Hermann, Alina</au><au>Henkel, Johanna</au><au>Seidel, Sebastian</au><au>Roitzheim, Christoph</au><au>Ksiazkiewicz, Agnieszka N</au><au>Hoffmann, Alexander</au><au>Pich, Andrij</au><au>Jones, Matthew D</au><au>Herres-Pawlis, Sonja</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactideElectronic supplementary information (ESI) available. CCDC 1880806-1880809. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt04938f</atitle><date>2019-05-07</date><risdate>2019</risdate><volume>48</volume><issue>18</issue><spage>671</spage><epage>682</epage><pages>671-682</pages><issn>1477-9226</issn><eissn>1477-9234</eissn><abstract>Non-toxic, highly active and robust complexes are the holy grail as ideal green catalysts for the polymerisation of biorenewable and biodegradable polylactide. Four new zinc guanidine complexes [ZnCl
2
(TMG4NMe
2
asme)], [ZnCl
2
(TMG5Clasme)], [ZnCl
2
(TMG5Measme)] and [ZnCl
2
(TMG5NMe
2
asme)] with different electron-donating and electron-withdrawing groups on the ligand's aromatic backbone have been synthesised. Ligands are derived from low-cost commercially available compounds and have been converted by a three- or four-step synthesis process into the desired ligand in good yields. The compounds have been fully characterised and tested in the ROP of
rac
-LA under industrially relevant conditions. The complexes are based on the recently published structure [ZnCl
2
(TMGasme)] which has shown high activity in the polymerisation of lactide at 150 °C. Different substituents in the
para
-position of the guanidine moiety significantly increase the polymerisation rate whereas positioning substituents in the
meta
-position causes no change in the reaction rate. With molecular weights over 71 000 g mol
−1
being achievable, the best system produces polymers for multiple industrial applications and its polymerisation rate approaches that of Sn(Oct)
2
. The robust systems are able to polymerise non-purified lactide. The initiation of the polymerisation is suggested to occur due to impurities in the monomer.
Four non-toxic, highly active and robust complexes have been used in the ring opening polymerisation of non-purifed lactide to substitute Sn(Oct)
2
.</abstract><doi>10.1039/c8dt04938f</doi><tpages>12</tpages></addata></record> |
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title | Tuning a robust system: N,O zinc guanidine catalysts for the ROP of lactideElectronic supplementary information (ESI) available. CCDC 1880806-1880809. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c8dt04938f |
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