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1‐Decene oligomerization by new complexes bearing diamine‐diphenolates ligands: Effect of ligand structure
A series of new titanium (IV) complexes bearing tetradentate diamine‐diphenolates, homologous to [ONNO] salan type ligands: [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC3H6NH}(Cl)2] (Cat1), [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC4H8NH}(Cl)2] (Cat2), and [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC6H4NH}(Cl)2] (Cat3) were synthesized and fu...
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Published in: | Applied organometallic chemistry 2021-06, Vol.35 (6), p.n/a |
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creator | Hanifpour, Ahad Bahri‐Laleh, Naeimeh Nekoomanesh‐Haghighi, Mehdi Poater, Albert |
description | A series of new titanium (IV) complexes bearing tetradentate diamine‐diphenolates, homologous to [ONNO] salan type ligands: [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC3H6NH}(Cl)2] (Cat1), [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC4H8NH}(Cl)2] (Cat2), and [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC6H4NH}(Cl)2] (Cat3) were synthesized and fully characterized by elemental analysis and NMR spectroscopy. All three synthesized catalysts, after activation with ([Ph3C][B(C6F5)4]) as a cocatalyst, exhibited high activities in 1‐decene oligomerization experiments. Gel permeation chromatography (GPC) analysis showed that molecular weight of the obtained oligomers had a close relationship with employed ligand structures, so that by increasing length of the aliphatic linkage between nitrogen donor atoms, PDI (Mw/Mn) shifted to the higher values. 1‐decene oligomers obtained by the Cat3 exhibited highest isotactic value (92% tacticity). Kinetic calculations allowed us to formulate the elementary reaction steps in oligomerization process of the 1‐decene. At the viscosity characterization, KV100 amounts of 2.9, 3.9, and 4.1 cSt were determined for synthesized oligomers with Cat1, Cat2, and Cat3, respectively. High catalyst activity, capability of producing PAOs with KV100 < 6, less toxicity and corrosiveness of the catalytic system (compared to commercialized process based on the hazardous BF3 catalyst), and simplicity of the preparation procedure are the merits of the new reported catalysts. |
doi_str_mv | 10.1002/aoc.6227 |
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All three synthesized catalysts, after activation with ([Ph3C][B(C6F5)4]) as a cocatalyst, exhibited high activities in 1‐decene oligomerization experiments. Gel permeation chromatography (GPC) analysis showed that molecular weight of the obtained oligomers had a close relationship with employed ligand structures, so that by increasing length of the aliphatic linkage between nitrogen donor atoms, PDI (Mw/Mn) shifted to the higher values. 1‐decene oligomers obtained by the Cat3 exhibited highest isotactic value (92% tacticity). Kinetic calculations allowed us to formulate the elementary reaction steps in oligomerization process of the 1‐decene. At the viscosity characterization, KV100 amounts of 2.9, 3.9, and 4.1 cSt were determined for synthesized oligomers with Cat1, Cat2, and Cat3, respectively. High catalyst activity, capability of producing PAOs with KV100 < 6, less toxicity and corrosiveness of the catalytic system (compared to commercialized process based on the hazardous BF3 catalyst), and simplicity of the preparation procedure are the merits of the new reported catalysts.</description><identifier>ISSN: 0268-2605</identifier><identifier>EISSN: 1099-0739</identifier><identifier>DOI: 10.1002/aoc.6227</identifier><language>eng</language><publisher>Chichester: Wiley Subscription Services, Inc</publisher><subject>1‐decene ; catalyst ; Catalysts ; Chemical analysis ; Chemical synthesis ; Chemistry ; Commercialization ; Coordination compounds ; Diamines ; Homology ; kinetic ; Ligands ; Liquid chromatography ; NMR spectroscopy ; Oligomerization ; Oligomers ; salan ; Tacticity ; Titanium ; Toxicity</subject><ispartof>Applied organometallic chemistry, 2021-06, Vol.35 (6), p.n/a</ispartof><rights>2021 John Wiley & Sons, Ltd.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3307-89a909eb47e7bfae349a2e0375adf3396b5ef062f65b7c98715caebc6129b2f63</citedby><cites>FETCH-LOGICAL-c3307-89a909eb47e7bfae349a2e0375adf3396b5ef062f65b7c98715caebc6129b2f63</cites><orcidid>0000-0002-8997-2599 ; 0000-0003-0696-7979 ; 0000-0002-6997-6787 ; 0000-0002-0925-5363</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Hanifpour, Ahad</creatorcontrib><creatorcontrib>Bahri‐Laleh, Naeimeh</creatorcontrib><creatorcontrib>Nekoomanesh‐Haghighi, Mehdi</creatorcontrib><creatorcontrib>Poater, Albert</creatorcontrib><title>1‐Decene oligomerization by new complexes bearing diamine‐diphenolates ligands: Effect of ligand structure</title><title>Applied organometallic chemistry</title><description>A series of new titanium (IV) complexes bearing tetradentate diamine‐diphenolates, homologous to [ONNO] salan type ligands: [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC3H6NH}(Cl)2] (Cat1), [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC4H8NH}(Cl)2] (Cat2), and [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC6H4NH}(Cl)2] (Cat3) were synthesized and fully characterized by elemental analysis and NMR spectroscopy. All three synthesized catalysts, after activation with ([Ph3C][B(C6F5)4]) as a cocatalyst, exhibited high activities in 1‐decene oligomerization experiments. Gel permeation chromatography (GPC) analysis showed that molecular weight of the obtained oligomers had a close relationship with employed ligand structures, so that by increasing length of the aliphatic linkage between nitrogen donor atoms, PDI (Mw/Mn) shifted to the higher values. 1‐decene oligomers obtained by the Cat3 exhibited highest isotactic value (92% tacticity). Kinetic calculations allowed us to formulate the elementary reaction steps in oligomerization process of the 1‐decene. At the viscosity characterization, KV100 amounts of 2.9, 3.9, and 4.1 cSt were determined for synthesized oligomers with Cat1, Cat2, and Cat3, respectively. High catalyst activity, capability of producing PAOs with KV100 < 6, less toxicity and corrosiveness of the catalytic system (compared to commercialized process based on the hazardous BF3 catalyst), and simplicity of the preparation procedure are the merits of the new reported catalysts.</description><subject>1‐decene</subject><subject>catalyst</subject><subject>Catalysts</subject><subject>Chemical analysis</subject><subject>Chemical synthesis</subject><subject>Chemistry</subject><subject>Commercialization</subject><subject>Coordination compounds</subject><subject>Diamines</subject><subject>Homology</subject><subject>kinetic</subject><subject>Ligands</subject><subject>Liquid chromatography</subject><subject>NMR spectroscopy</subject><subject>Oligomerization</subject><subject>Oligomers</subject><subject>salan</subject><subject>Tacticity</subject><subject>Titanium</subject><subject>Toxicity</subject><issn>0268-2605</issn><issn>1099-0739</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2021</creationdate><recordtype>article</recordtype><recordid>eNp1kE1OwzAQRi0EEqUgcQRLbNik2E7ixOyqUn6kSt3AOnKccXGV2MFOVcqKI3BGToKh3bIa6Zv3zUgPoUtKJpQQdiOdmnDGiiM0okSIhBSpOEYjwniZME7yU3QWwpoQIjjNRsjS78-vO1BgAbvWrFwH3nzIwTiL6x22sMXKdX0L7xBwDdIbu8KNkZ2xEJuN6V_BulYOcR3r0jbhFs-1BjVgpw8RDoPfqGHj4RydaNkGuDjMMXq5nz_PHpPF8uFpNl0kKk1JkZRCCiKgzgooai0hzYRkQNIil41OU8HrHDThTPO8LpQoC5orCbXilIk6pukYXe3v9t69bSAM1dptvI0vK5YzzkmZZVmkrveU8i4ED7rqvemk31WUVL82q2iz-rUZ0WSPbk0Lu3-5arqc_fE_RyF5Qg</recordid><startdate>202106</startdate><enddate>202106</enddate><creator>Hanifpour, Ahad</creator><creator>Bahri‐Laleh, Naeimeh</creator><creator>Nekoomanesh‐Haghighi, Mehdi</creator><creator>Poater, Albert</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0002-8997-2599</orcidid><orcidid>https://orcid.org/0000-0003-0696-7979</orcidid><orcidid>https://orcid.org/0000-0002-6997-6787</orcidid><orcidid>https://orcid.org/0000-0002-0925-5363</orcidid></search><sort><creationdate>202106</creationdate><title>1‐Decene oligomerization by new complexes bearing diamine‐diphenolates ligands: Effect of ligand structure</title><author>Hanifpour, Ahad ; Bahri‐Laleh, Naeimeh ; Nekoomanesh‐Haghighi, Mehdi ; Poater, Albert</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3307-89a909eb47e7bfae349a2e0375adf3396b5ef062f65b7c98715caebc6129b2f63</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2021</creationdate><topic>1‐decene</topic><topic>catalyst</topic><topic>Catalysts</topic><topic>Chemical analysis</topic><topic>Chemical synthesis</topic><topic>Chemistry</topic><topic>Commercialization</topic><topic>Coordination compounds</topic><topic>Diamines</topic><topic>Homology</topic><topic>kinetic</topic><topic>Ligands</topic><topic>Liquid chromatography</topic><topic>NMR spectroscopy</topic><topic>Oligomerization</topic><topic>Oligomers</topic><topic>salan</topic><topic>Tacticity</topic><topic>Titanium</topic><topic>Toxicity</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hanifpour, Ahad</creatorcontrib><creatorcontrib>Bahri‐Laleh, Naeimeh</creatorcontrib><creatorcontrib>Nekoomanesh‐Haghighi, Mehdi</creatorcontrib><creatorcontrib>Poater, Albert</creatorcontrib><collection>CrossRef</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Applied organometallic chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hanifpour, Ahad</au><au>Bahri‐Laleh, Naeimeh</au><au>Nekoomanesh‐Haghighi, Mehdi</au><au>Poater, Albert</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>1‐Decene oligomerization by new complexes bearing diamine‐diphenolates ligands: Effect of ligand structure</atitle><jtitle>Applied organometallic chemistry</jtitle><date>2021-06</date><risdate>2021</risdate><volume>35</volume><issue>6</issue><epage>n/a</epage><issn>0268-2605</issn><eissn>1099-0739</eissn><abstract>A series of new titanium (IV) complexes bearing tetradentate diamine‐diphenolates, homologous to [ONNO] salan type ligands: [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC3H6NH}(Cl)2] (Cat1), [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC4H8NH}(Cl)2] (Cat2), and [Ti{2,2′‐(OC6H2–4,6‐tBu2)2NHC6H4NH}(Cl)2] (Cat3) were synthesized and fully characterized by elemental analysis and NMR spectroscopy. All three synthesized catalysts, after activation with ([Ph3C][B(C6F5)4]) as a cocatalyst, exhibited high activities in 1‐decene oligomerization experiments. Gel permeation chromatography (GPC) analysis showed that molecular weight of the obtained oligomers had a close relationship with employed ligand structures, so that by increasing length of the aliphatic linkage between nitrogen donor atoms, PDI (Mw/Mn) shifted to the higher values. 1‐decene oligomers obtained by the Cat3 exhibited highest isotactic value (92% tacticity). Kinetic calculations allowed us to formulate the elementary reaction steps in oligomerization process of the 1‐decene. At the viscosity characterization, KV100 amounts of 2.9, 3.9, and 4.1 cSt were determined for synthesized oligomers with Cat1, Cat2, and Cat3, respectively. High catalyst activity, capability of producing PAOs with KV100 < 6, less toxicity and corrosiveness of the catalytic system (compared to commercialized process based on the hazardous BF3 catalyst), and simplicity of the preparation procedure are the merits of the new reported catalysts.</abstract><cop>Chichester</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aoc.6227</doi><tpages>13</tpages><orcidid>https://orcid.org/0000-0002-8997-2599</orcidid><orcidid>https://orcid.org/0000-0003-0696-7979</orcidid><orcidid>https://orcid.org/0000-0002-6997-6787</orcidid><orcidid>https://orcid.org/0000-0002-0925-5363</orcidid></addata></record> |
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subjects | 1‐decene catalyst Catalysts Chemical analysis Chemical synthesis Chemistry Commercialization Coordination compounds Diamines Homology kinetic Ligands Liquid chromatography NMR spectroscopy Oligomerization Oligomers salan Tacticity Titanium Toxicity |
title | 1‐Decene oligomerization by new complexes bearing diamine‐diphenolates ligands: Effect of ligand structure |
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