About: Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles

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About: Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles Goto Sponge NotDistinct Permalink

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scientific article published on 01 August 2010

Attributes	Values
rdf:type	Item
description	wetenschappelijk artikel (nl) наукова стаття, опублікована в серпні 2010 (uk) artículu científicu espublizáu n'agostu de 2010 (ast) scientific article published on 01 August 2010 (en)
publication date	wds:Q84646983-0ACEA3C9-C77B-4410-A72F-70F6F30CD9A2
publication date	2010-08-01 00:00:00Z (xsd:dateTime)
language of work or name	wds:Q84646983-CD50B65F-4614-4783-AF02-526D2C18D79A
language of work or name	English
cites work	wds:Q84646983-419D1361-8F6D-4D61-92E8-F69EA9D9114C
cites work	Amide-based molecular shuttles (2001-2006)
author name string	wds:Q84646983-6F2F1EA4-A831-4263-AD6F-D2149DB1E256 wds:Q84646983-D818C1A2-3466-4E8E-86C6-8CF267EEF66B
author name string	Mateo Alajarín Raúl-Angel Orenes
rdfs:label	Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (en) Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (nl)
skos:prefLabel	Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (en) Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (nl)
name	Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (en) Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (nl)
author	wds:Q84646983-DF30E197-9D24-403E-9C9D-6EC674B6C0B2
author	José Berna
title	wds:Q84646983-9E8AC4A9-5CD4-44DD-99CA-93465308CFF3
title	Azodicarboxamides as template binding motifs for the building of hydrogen-bonded molecular shuttles (en)
page(s)	wds:Q84646983-2AEADA34-0961-44AB-8B65-49CB74F4EC62
page(s)	10741-10747
instance of	wds:Q84646983-EC3580EA-34DE-46F6-B1C7-F27A52F18FA7
instance of	scholarly article
PubMed ID	wds:Q84646983-D922ED54-C088-4415-A739-F95FB34F33AE
PubMed ID	http://rdf.ncbi.nlm.nih.gov/pubchem/reference/20681706
PubMed ID	20681706
published in	wds:Q84646983-6C0E30AA-078F-4812-A379-699C533B9AD6
published in	Journal of the American Chemical Society
issue	wds:Q84646983-B123CCDE-83AF-48C6-9505-C73F1A6AD45E
volume	wds:Q84646983-CB4D1D43-3C8B-4D6B-A212-F3BF2587B72C
issue	31
volume	132
DOI	wds:Q84646983-ABED310B-7FB1-4A5D-B834-A28D7337D633
DOI	http://dx.doi.org/10.1021/JA101151T
DOI	10.1021/JA101151T
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q84646983
is cites work of	Artificial Molecular Machines Fuel-Controlled Reassembly of Metal-Organic Architectures Reversible light switch for macrocycle mobility in a DNA rotaxane A Stimuli-Responsive Rotaxane-Gold Catalyst: Regulation of Activity and Diastereoselectivity. Asymmetric Catalysis with a Mechanically Point-Chiral Rotaxane Redox-Dependent Conformational Switching of Diphenylacetylenes Reversible mechanical switching of magnetic interactions in a molecular shuttle High yielding synthesis of 2,2'-bipyridine macrocycles, versatile intermediates in the synthesis of rotaxanes. A robust binary supramolecular organic framework (SOF) with high CO2 adsorption and selectivity. Versatile control of the submolecular motion of di(acylamino)pyridine-based [2]rotaxanes. The tris-urea motif and its incorporation into polydimethylsiloxane-based supramolecular materials presenting self-healing features Photoinduced Pedalo-Type Motion in an Azodicarboxamide-Based Molecular Switch. Co-conformational Exchange Triggered by Molecular Recognition in a Di(acylamino)pyridine-Based Molecular Shuttle Containing Two Pyridine Rings at the Macrocycle. Effects on Rotational Dynamics of Azo and Hydrazodicarboxamide-Based Rotaxanes. Photoswitchable interlocked thiodiglycolamide as a cocatalyst of a chalcogeno-Baylis-Hillman reaction. Dissipative Catalysis with a Molecular Machine. Molecular recognition using tetralactam macrocycles with parallel aromatic sidewalls.
is cites work of	wds:Q41990480-F714AC1D-8736-42C5-B0ED-79BC9DD19AE6 wds:Q27300746-AF57B525-356C-4181-A1DD-CC0212B91CEF wds:Q36722665-1F85E4CA-82FC-4B16-ABD6-F9AB49564D5C wds:Q48302053-AD41EE20-E4FC-4467-B1DB-24E44AF892A4 wds:Q53191584-9FE7E8A2-C5DC-4E6F-A71D-EDE4813E1440 wds:Q86783243-B291889B-9CDC-47C7-BB7B-6E31E49E2F26 wds:Q26783064-CAD1BDA3-DDB7-480A-ABB3-192AF1E1DA76 wds:Q42257922-ACE5E54C-6B3B-47E3-BAD9-88508C978D56 wds:Q36369933-BA0BF51E-F4BA-4C46-99C4-7DECDAB5BB69 wds:Q41008059-0232B94D-24E3-4A96-8B74-ECD34D0A4E1B wds:Q42249060-ACB734FF-83CC-4694-9D81-0B35111CAE57 wds:Q48044719-9D43561C-C58B-4B1D-8711-57F110888173 wds:Q55626098-E11D4B3E-C985-41B2-B748-61DDFF17E833 wds:Q34282617-5E3C0C47-5E61-4F25-AEE1-2E2CB2DE55E4 wds:Q64017512-04E691E1-FF07-418F-A352-EE413ACAF27F wds:Q58213204-9504CAD5-2202-4F6C-ABAA-732226BD8C10 wds:Q64990872-673EA177-D16A-447F-8B9C-CAF466C318EF

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