Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer. - Wikidata - awgldk - TriplyDB

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

http://www.wikidata.org/entity/Q30882378

about

Photoswitchable Carbohydrate-Based Macrocyclic Azobenzene: Synthesis, Chiroptical Switching, and Multistimuli-Responsive Self-Assembly.Azo group(s) in selected macrocyclic compounds.Light-responsive molecular containers.

P2860

Q48146783-D60C3B47-8C92-441B-B843-514C72101DD9 Q52930229-A5618649-CA40-4611-A25E-878D0B6E7909 Q53632627-778C928A-87AC-4EAB-AFCF-81AC1D319BD9

P2860

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

http://www.wikidata.org/entity/Q30882378

description

2014 nî lūn-bûn

@nan

2014 թուականի Դեկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2014 թվականի դեկտեմբերին հրատարակված գիտական հոդված

@hy

2014年の論文

@ja

2014年学术文章

@wuu

2014年学术文章

@zh-cn

2014年学术文章

@zh-hans

2014年学术文章

@zh-my

2014年学术文章

@zh-sg

2014年學術文章

@yue

name

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@ast

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@en

type

label

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@ast

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@en

prefLabel

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@ast

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer.

@en

P1433

Q30882378-C4778B5B-4A3A-4CA5-9B5C-E9356FF36BD1

P1476

Q30882378-8C0A8DC5-F7D6-4E89-8586-E2AF7BF01EE9

P2093

Q30882378-20EEDE9E-4F80-4AB9-9BA0-01041D47DC59

Q30882378-3D81EBA2-2C79-494E-8532-7B420814E471

Q30882378-5BB6A58F-EC6F-46A8-B6AB-15CE90493530

Q30882378-63A245F9-3036-4285-AC86-26FA2902C49B

Q30882378-6FEAF38C-C38E-4BC0-A24C-82DB1ECA1FAD

Q30882378-7BD1F9DD-AFF0-4B10-AA81-4A759BC72F2C

P2860

Q30882378-017673D3-F232-47B2-81F9-D9B1986C65D8

Q30882378-0F3633AD-C7FC-43E8-BA58-0B06A1F0C275

Q30882378-118C3244-53C7-474C-B147-68EF64CE11DF

Q30882378-11B4458F-292B-4103-8682-9D00A5B4F63D

Q30882378-275FB005-B6E5-4CE2-8106-7E6CF5F5CA53

Q30882378-36E890FB-AC9B-4BF8-865E-4A1B3897859E

Q30882378-4963C03B-3A08-418D-AB31-ED4B3BC8B66B

Q30882378-55594ABD-8E95-40F0-8584-DB93695273A3

Q30882378-81A9F051-E663-409A-AEA4-CE535D47429A

Q30882378-983F7ABD-B30D-46B5-A2E9-2682BE9A8FE7

P304

Q30882378-759BE4BC-8548-4C74-AFF3-980C8EF6B463

P31

Q30882378-51A525BC-CBB5-4C58-85BD-9BFB4C1895F7

P356

Q30882378-17320102-0048-4461-AE60-B2E36589FF24

P478

Q30882378-4AD260FD-B0F9-4BE1-853B-5961CAAB47C4

P50

Q30882378-40B04B68-1F8F-43B4-92EF-03828426C0BD

Q30882378-CD462FB0-2F32-4668-9FA0-0B5043141B5D

Q30882378-CDCFB7B8-3E68-477F-8A76-28732C3F2102

Q30882378-D14415C8-7925-422B-ADEB-753ED7951118

Q30882378-D3A1CD36-7500-4467-B0D8-151E589E637B

P577

Q30882378-4FF45CB7-FDED-4C98-BD9B-2E48FE8FA7A9

P5875

Q30882378-2C94D76E-6F1A-45AD-A3A5-F23D4023781D

P698

Q30882378-54E8A86F-A873-4443-A38C-C2E1E0AF6585

P932

Q30882378-9112544E-207B-4488-8983-51CC33016598

P356

P1433

Beilstein Journal of Organic Chemistry

P1476

Synthesis and characterization of a new photoinduced switchable β-cyclodextrin dimer

@en

P2093

Christine Cézard

http://www.w3.org/2001/XMLSchema#string

Claire Blaszkiewicz

http://www.w3.org/2001/XMLSchema#string

Estelle Banaszak-Léonard

http://www.w3.org/2001/XMLSchema#string

Florence Djedaini-Pilard

http://www.w3.org/2001/XMLSchema#string

Florian Hamon

http://www.w3.org/2001/XMLSchema#string

Marie Buchotte

http://www.w3.org/2001/XMLSchema#string

P2860

R.E.DD.B.: a database for RESP and ESP atomic charges, and force field libraries

R.E.D. Server: a web service for deriving RESP and ESP charges and building force field libraries for new molecules and molecular fragments.

Physico-chemical investigation of asymmetrical peptidolipidyl-cyclodextrins.

The R.E.D. tools: advances in RESP and ESP charge derivation and force field library building.

Cooperative binding and stabilization of the medicinal pigment curcumin by diamide linked γ-cyclodextrin dimers: a spectroscopic characterization.

Molecular dynamics studies of native and substituted cyclodextrins in different media: 1. Charge derivation and force field performances.

Cis-trans isomerization of organic molecules and biomolecules: implications and applications.

Pharmaceutical applications of cyclodextrins: basic science and product development.

How to conduct and interpret ITC experiments accurately for cyclodextrin-guest interactions.

Control over molecular motion using the cis-trans photoisomerization of the azo group.

P304

2874-2885

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.3762/BJOC.10.304

http://www.w3.org/2001/XMLSchema#string

P478

10

http://www.w3.org/2001/XMLSchema#string

P50

Sebastien Tilloy

Laurent Bouteiller

P577

2014-12-04T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

270289988

http://www.w3.org/2001/XMLSchema#string

P698

25550753

http://www.w3.org/2001/XMLSchema#string

P932

4273303

http://www.w3.org/2001/XMLSchema#string