کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1321588 1499826 2016 13 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Alkoxido-, amido-, and chlorido derivatives of zirconium- and hafnium bis(amido)cyclodiphosph(V)azanes: Ligand ambidenticity and catalytic productivity
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی معدنی
پیش نمایش صفحه اول مقاله
Alkoxido-, amido-, and chlorido derivatives of zirconium- and hafnium bis(amido)cyclodiphosph(V)azanes: Ligand ambidenticity and catalytic productivity
چکیده انگلیسی


• κ2N,N′-Bis(tert-butylamido)cyclodiphosph(III)azanezirconium dichloride polymerizes ethylene.
• The catalyst deactivates due to Lewis-acid attack on the phosphorus(III) centers.
• A bis(tert-butylamido)cyclodiphosph(V)azane ligand yields an inactive κN,κS catalyst.
• Oxidation of the original catalyst with sulfur generates a more productive κ2N,N'catalyst.

Bis(tert-butylamido)cyclodiphosph(III)azanezirconium- and hafnium dichloride are good polyethylene pre-catalysts, but due to the basicity of their phosphorus(III) atoms they suffer from ligand degradation. To lessen the Lewis-acid attacks on these complexes, the phosphorus-nitrogen ligands were oxidized with sulfur to afford the corresponding bis(tert-butylamido)cyclodiphosph(V)azanes, which are devoid of such very Lewis-basic sites. These modified ligands, however, no longer bind the metals in the desired κ2N,N′ fashion, but laterally in the catalytically inactive κN,κEl mode. Treatment of the Group 4 metal dichlorides with sodium tert-butoxide afforded the bis(tert-butylamido)cyclodiphosph(III)azanemetal di-tert-butoxides in high yields. These compounds were amenable to sulfur oxidation, yielding bis(tert-butylamido)cyclodiphosph(V)azanemetal di-tert-butoxides in equally high yields. The oxidized complexes retain the κ2N,N′ structure, prompting us to reinvestigate a similar oxidation of the bis(tert-butylamido)cyclodiphosph(III)azanemetal dichlorides. The dichloride complexes were more difficult to oxidize, but ultimately bis(tert-butylamido)cyclodiphosph(V)azanezirconium- and hafnium dichlorides were obtained and shown to be more productive catalysts than their phosphorus(III) counterparts.

Bis(tert-butylamido)cyclodiphosph(III)azanezirconium dichloride is an active polyethylene catalyst, but its Lewis-basic phosphorus atoms make it susceptible to degradation. Ligand oxidation with sulfur prior to metalation produces an inactive κN,κS zirconium complex. Oxidation after metalation retains the original κ2N,N′ structure and generates a more productive catalyst.Figure optionsDownload as PowerPoint slide

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Organometallic Chemistry - Volume 820, 1 October 2016, Pages 98–110
نویسندگان
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