About: Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group

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About: Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group Goto Sponge Distinct Permalink

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scholarly article by Takuzo Aida & Shohei Inoue published March 1983 in Journal of the American Chemical Society

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в березні 1983 (uk) im März 1983 veröffentlichter wissenschaftlicher Artikel (de) scholarly article by Takuzo Aida & Shohei Inoue published March 1983 in Journal of the American Chemical Society (en)
publication date	wds:Q56679238-4829412A-4B18-471F-BE2E-3A42AF1CA230
publication date	1983-03-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q56679238-3288E948-004A-458D-BD5F-A0FACD93AE4E
language of work or name	English
rdfs:label	Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (nl) Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group (en)
skos:prefLabel	Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (nl) Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group (en)
name	Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (nl) Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group (en)
author	wds:Q56679238-5471A4F9-0673-463C-A32B-AA2F13161D13 wds:Q56679238-8478FDD8-0AC1-4FBF-BA26-45996878CB64
author	Takuzo Aida Shohei Inoue
title	wds:Q56679238-1DE7D815-510E-4AC8-A1F8-BF1DFD054959
title	Activation of carbon dioxide with aluminum porphyrin and reaction with epoxide. Studies on (tetraphenylporphinato)aluminum alkoxide having a long oxyalkylene chain as the alkoxide group (en)
page(s)	wds:Q56679238-E57EEC36-6F1F-4BEB-8258-912B5A2757A3
page(s)	1304-1309
instance of	wds:Q56679238-B05C394B-474F-4A3D-BE24-7E85019BA63C
instance of	scholarly article
main subject	wds:Q56679238-672b45f6-8628-4de0-bf67-26010c5d6764
main subject	aluminium
published in	wds:Q56679238-970A5C35-3A3F-4547-BE3F-FC3A8ADD0D0D
published in	Journal of the American Chemical Society
issue	wds:Q56679238-7E7A8B9C-5674-4E67-B1DD-79278BA3BBF1
volume	wds:Q56679238-6F1FA296-42E2-4461-952F-252DB9FFD80C
issue	5
volume	105
DOI	wds:Q56679238-826CCCAB-041A-49FC-ADC3-BA3C9D4B182C
DOI	http://dx.doi.org/10.1021/JA00343A038
DOI	10.1021/JA00343A038
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q56679238
is cites work of	Unprecedented Carbonato Intermediates in Cyclic Carbonate Synthesis Catalysed by Bimetallic Aluminium(Salen) Complexes. Aluminium salabza complexes for fixation of CO2 to organic carbonates. Glycerol carbonate as a versatile building block for tomorrow: synthesis, reactivity, properties and applications Using carbon dioxide as a building block in organic synthesis Catalysts for CO2/epoxide ring-opening copolymerization Synthesis of cyclic carbonates from epoxides and carbon dioxide by using organocatalysts A Water-Stable Porphyrin-Based Metal-Organic Framework Active for Visible-Light Photocatalysis Selective Synthesis of Cyclic Carbonate by Salalen-Aluminum Complexes and Mechanistic Studies Metal-catalyzed synthesis of alternating copolymers A MALDI-TOF MS analysis study of the binding of 4-(N,N-dimethylamino)pyridine to amine-bis(phenolate) chromium(III) chloride complexes: mechanistic insight into differences in catalytic activity for CO2/epoxide copolymerization. Highly Active and Robust Metalloporphyrin Catalysts for the Synthesis of Cyclic Carbonates from a Broad Range of Epoxides and Carbon Dioxide. Biodegradable poly(carbonate-ether)s with thermoresponsive feature at body temperature Renaissance of Aliphatic Polycarbonates: New Techniques and Biomedical Applications Bifunctional Ionic Liquids Derived from Biorenewable Sources as Sustainable Catalysts for Fixation of Carbon Dioxide CO2 Capture by 2-(Methylamino)pyridine Ligated Aluminum Alkyl Complexes A DFT Study on the Co-polymerization of CO2 and Ethylene: Feasibility Analysis for the Direct Synthesis of Polyethylene Esters. Ethylene Oxide Aluminum complexes derived from a hexadentate salen-type Schiff base: synthesis, structure, and catalysis for cyclic carbonate synthesis Hydrophilic CO2-based biodegradable polycarbonates: Synthesis and rapid thermo-responsive behavior Challenges and Opportunities in Synthesizing High Volume Chemicals from CO2 without Direct H2 Input CO2 Fixation with Epoxides under Mild Conditions with a Cooperative Metal Corrole/Quaternary Ammonium Salt Catalyst System. Highly Selective Single-Component Formazanate Ferrate(II) Catalysts for the Conversion of CO2 into Cyclic Carbonates
is cites work of	wds:Q26769629-5E8F260C-FDD4-4281-9657-139FFDA268FD wds:Q38539618-1FE1B22C-3C26-4DA0-BF49-2F8C160BA068 wds:Q53344208-9519C9ED-416E-4FF4-A3AA-856A3AF03CCD wds:Q98907125-969E8895-D35B-4503-868F-E217FC80AB0D wds:Q46452787-FB19019A-1C80-48B5-BCA2-8AB68BC55321 wds:Q48041982-2A41EDAB-CC9A-4A2B-8670-829DC1D83A9B wds:Q55918649-47E651C9-FB7A-4938-A248-D1C9D43B3095 wds:Q57915634-6653E9A3-6F9B-4CE1-944F-67B770A8D36B wds:Q53094229-E85C3B8E-0F1B-4281-AEF0-966D106EA425 wds:Q57352740-CE3C3D55-17FA-4E6B-99F0-EF2D44FCD737 wds:Q59318728-2C193410-4E97-4FE7-86C7-11108A2AAD86 wds:Q99569045-222BF39F-A215-4FEF-8957-A3993C5CFBF7 wds:Q33469057-63AF7F3E-DCD5-4FDF-A6C8-43B605543C1C wds:Q37857074-E6D869DA-98DF-4E98-9824-4696DA8F64CC wds:Q91640116-BB938037-8D5E-4E6B-8C24-8CDE39678113 wds:Q33470267-FA6FAB9A-E338-4187-A7ED-CB15BA17C125 wds:Q42241632-EC37A577-E22B-43A7-8D3E-5A48EBD01B9F wds:Q50230746-A1E33DE4-42B0-4A8A-8C98-ED8C448787A9 wds:Q46785110-A176A82E-2034-4333-A31E-D0AB433E2B21 wds:Q57352814-98B9F0B0-CCC7-4A37-A1AB-96E4F88B0821 wds:Q33826053-D7199E07-AA94-47A5-97E1-AD21A0249C51 wds:Q46577717-E3ECBD57-D558-4E03-B022-CBDFDE56EA9B

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