Structure–property relationship studies of 3-acyl-substituted furans: the serendipitous identification and characterization of a new non-classical hydrogen bond donor moiety

2020 ◽  
Vol 44 (26) ◽  
pp. 10994-11005
Author(s):  
Daniel A. Rodrigues ◽  
Pedro de Sena M. Pinheiro ◽  
Fernanda S. Sagrillo ◽  
Maria Clara R. Freitas ◽  
Marina A. Alves ◽  
...  
Keyword(s):  
Hydrogen Bond ◽  
Structure Property ◽  
Hydrogen Bond Donor ◽  
Property Relationship ◽  
Structure Property Relationship ◽  
Classical Hydrogen Bond ◽  
Donor Moiety ◽  
Identification And Characterization ◽  
Substituted Furans

A serendipitous identification and characterization of a new non-classical hydrogen bond donor moiety found in N-acylhydrazones containing 3-acyl-substituted furan subunit is presented.

Implications of the structure-property relationship on the optomechanical characterization of the cornea: A review

Optik ◽  
2021 ◽  
Vol 232 ◽  
pp. 166529
Author(s):  
Himanshu Gururani ◽  
Ashutosh Richhariya ◽  
Ramji M. ◽  
Viswanath Chinthapenta
Keyword(s):  
Structure Property ◽  
Property Relationship ◽  
Structure Property Relationship

A structure–property relationship study of bent-core mesogens with pyridine as the central unit

2014 ◽  
Vol 38 (4) ◽  
pp. 1751-1760 ◽  
Author(s):  
J. M. Marković ◽  
N. P. Trišović ◽  
T. Tóth-Katona ◽  
M. K. Milčić ◽  
A. D. Marinković ◽  
...  
Keyword(s):  
Liquid Crystals ◽  
Pyridine Ring ◽  
Synthesis And Characterization ◽  
Central Unit ◽  
Structure Property ◽  
Aromatic Rings ◽  
Property Relationship ◽  
Structure Property Relationship ◽  
Relationship Study

The synthesis and characterization of pyridine bent-core liquid crystals are reported. Some compounds exhibit B1 and B7 mesophases. Lower and wider mesophase ranges are obtained by decreasing the polarity of linkers between the pyridine ring and the inner aromatic rings, and increasing the length of terminal chains.

scholarly journals Asymmetric multifunctional 3D cell microenvironments by capillary force assembly

2019 ◽  
Vol 7 (22) ◽  
pp. 3560-3568
Author(s):  
Qimeng Song ◽  
Sergey I. Druzhinin ◽  
Holger Schönherr
Keyword(s):  
Cell Culture ◽  
Capillary Force ◽  
3D Cell Culture ◽  
Structure Property ◽  
Property Relationship ◽  
Structure Property Relationship ◽  
Systematic Structure ◽  
Fabrication And Characterization

The fabrication and characterization of advanced 3D cell culture microenvironments that enable systematic structure–property relationship studies are reported.

Synthesis and Characterization of Soluble Phthalocyanines: Structure-Property Relationship

1990 ◽  
Vol 187 (1) ◽  
pp. 365-382 ◽  
Author(s):  
Michael Hanack ◽  
Ahmet Gül ◽  
Andreas Hirsch ◽  
Braja K. Mandal ◽  
L. R. Subramanian ◽  
...  
Keyword(s):  
Synthesis And Characterization ◽  
Structure Property ◽  
Property Relationship ◽  
Structure Property Relationship

1,4:3,6-Dianhydrohexitols: Original platform for the design of biobased polymers using robust, efficient, and orthogonal chemistry

2012 ◽  
Vol 85 (3) ◽  
pp. 511-520 ◽  
Author(s):  
Pascal Dimitrov Raytchev ◽  
Céline Besset ◽  
Etienne Fleury ◽  
Jean-Pierre Pascault ◽  
Julien Bernard ◽  
...  
Keyword(s):  
Polymer Materials ◽  
Structure Property ◽  
Materials Properties ◽  
Property Relationship ◽  
Biobased Polymers ◽  
Structure Property Relationship ◽  
Step Growth ◽  
Step Growth Polymerization ◽  
The Impact

1,4:3,6-Dianhydrohexitols (DAHs) are nontoxic and sustainable diols that have been extensively applied as monomers for the preparation of polymer materials by step-growth polymerization processes. The presence of two reactive alcohol groups was exploited to design a library of symmetric and asymmetric stereocontrolled alkyne- and/or azide-functionalized AA/BB and AB monomers suitable for thermal or copper(I)-catalyzed azide-alkyne cycloaddition (TAAC and CuAAC). Step-growth polymerization of these monomers yielded a series of linear polytriazoles as well as partially biosourced networks using a combination of AB + A2B2 derivatives. Characterization of the resulting materials allowed for the establishment of a thorough structure–property relationship emphasizing the impact of monomer stereochemistry and cycloaddition regioselectivity on materials properties.

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