scholarly journals Tuning the Properties of Hydrogen-bonded Block Copolymer Worm Gels Prepared via Polymerization-Induced Self-Assembly

2021 ◽  
Author(s):  
Eleanor Raphael ◽  
Matthew J Derry ◽  
Michael Hippler ◽  
Steven P Armes
Keyword(s):  
Hydrogen Bonding ◽  
Carboxylic Acid ◽  
Block Copolymer ◽  
Self Assembly ◽  
Raft Agent ◽  
Stearyl Methacrylate ◽  
Hydrogen Bonded

Polymerization-induced self-assembly (PISA) is exploited to design hydrogen-bonded poly(stearyl methacrylate)-poly(benzyl methacrylate) [PSMA-PBzMA] worm gels in n-dodecane. Using a carboxylic acid-based RAFT agent facilitates hydrogen bonding between neighboring worms to produce...

Mesoporous Block Copolymer Nanoparticles with Tailored Structures by Hydrogen-Bonding-Assisted Self-Assembly

2012 ◽  
Vol 24 (14) ◽  
pp. 1889-1893 ◽  
Author(s):  
Renhua Deng ◽  
Shanqin Liu ◽  
Jingyi Li ◽  
Yonggui Liao ◽  
Juan Tao ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Block Copolymer ◽  
Self Assembly

Cinnamic acid hydrogen bonds to isoniazid andN′-(propan-2-ylidene)isonicotinohydrazide, anin situreaction product of isoniazid and acetone

2014 ◽  
Vol 70 (4) ◽  
pp. 392-395 ◽  
Author(s):  
Inese Sarcevica ◽  
Liana Orola ◽  
Mikelis V. Veidis ◽  
Sergey Belyakov
Keyword(s):  
Crystal Structure ◽  
Hydrogen Bonding ◽  
Carboxylic Acid ◽  
Hydrogen Bonds ◽  
Cinnamic Acid ◽  
Slow Evaporation ◽  
Hydrogen Bonded

A new polymorph of the cinnamic acid–isoniazid cocrystal has been prepared by slow evaporation, namely cinnamic acid–pyridine-4-carbohydrazide (1/1), C9H8O2·C6H7N3O. The crystal structure is characterized by a hydrogen-bonded tetrameric arrangement of two molecules of isoniazid and two of cinnamic acid. Possible modification of the hydrogen bonding was investigated by changing the hydrazide group of isoniazidviaanin situreaction with acetone and cocrystallization with cinnamic acid. In the structure of cinnamic acid–N′-(propan-2-ylidene)isonicotinohydrazide (1/1), C9H8O2·C9H11N3O, carboxylic acid–pyridine O—H...N and hydrazide–hydrazide N—H...O hydrogen bonds are formed.

Nano-structuring polymer/fullerene composites through the interplay of conjugated polymer crystallization, block copolymer self-assembly and complementary hydrogen bonding interactions

2015 ◽  
Vol 6 (5) ◽  
pp. 721-731 ◽  
Author(s):  
Fei Li ◽  
Kevin G. Yager ◽  
Noel M. Dawson ◽  
Ying-Bing Jiang ◽  
Kevin J. Malloy ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Block Copolymer ◽  
Supramolecular Chemistry ◽  
Self Assembly ◽  
Conjugated Polymer ◽  
Composite Nanofibers ◽  
Core Shell ◽  
Hydrogen Bonding Interactions ◽  
Non Covalent Interactions ◽  
Covalent Interactions

Core–shell P3HT/fullerene composite nanofibers were obtained using supramolecular chemistry involving cooperative orthogonal non-covalent interactions.

Irᴵᴵᴵ as a Strategy for Preorganization in H-Bonded Motifs

2019 ◽  
Author(s):  
Barbora Balonova ◽  
Helena J. Shepherd ◽  
Christopher Serpell ◽  
Barry Blight
Keyword(s):  
Hydrogen Bonding ◽  
Metal Complexes ◽  
General Formula ◽  
Self Assembly ◽  
Structural Design ◽  
Functional Materials ◽  
Soft Materials ◽  
Thiourea Derivatives ◽  
Hydrogen Bonded Systems ◽  
Hydrogen Bonded

Here we present the synthesis and characterisation of four hydrogen bonded systems based on thiourea derivatives. These motifs are considered to be stable and desirable for supramolecular hydrogen-bonded functional materials. Interpretation of the structural design of thiourea based ligand and its incorporation into metal complexes can contribute to the understanding of preorganised self-assembly and open new pathways in design of novel soft materials. This work contributes to the unexplored library of hydrogen bonded metal complexes based on iridium. Further we examined the photoluminescence of the system of general formula [Ir(C^N)<sub>2</sub>(N^S)] and the effect of hydrogen bonding on the emission properties when combined with different <i>n</i>-heteroacenes.

Exocyclic self-assembly behavior of carboxylic acid and lariat ether macrocyclic hosts: regulation by pendent arm

RSC Advances ◽  
2015 ◽  
Vol 5 (84) ◽  
pp. 68864-68874
Author(s):  
Rong Guo ◽  
Wei Wang ◽  
Weiping Yang ◽  
Yuanyin Chen ◽  
Shuling Gong
Keyword(s):  
Hydrogen Bonding ◽  
Carboxylic Acid ◽  
Self Assembly ◽  
Building Block ◽  
Hydrogen Bonding Interaction ◽  
Lariat Ether ◽  
Diazacrown Ethers ◽  
Bonding Interaction ◽  
Assembly Behavior

An exocyclic supramolecular building block through O–H⋯N hydrogen bonding interaction for the assembly of di-sidearm dibenzo-diazacrown ethers bearing a flexibility sidearm with PTA acid.

Irᴵᴵᴵ as a Strategy for Preorganization in H-Bonded Motifs

2019 ◽  
Author(s):  
Barbora Balonova ◽  
Helena J. Shepherd ◽  
Christopher Serpell ◽  
Barry Blight
Keyword(s):  
Hydrogen Bonding ◽  
Metal Complexes ◽  
General Formula ◽  
Self Assembly ◽  
Structural Design ◽  
Functional Materials ◽  
Soft Materials ◽  
Thiourea Derivatives ◽  
Hydrogen Bonded Systems ◽  
Hydrogen Bonded

Here we present the synthesis and characterisation of four hydrogen bonded systems based on thiourea derivatives. These motifs are considered to be stable and desirable for supramolecular hydrogen-bonded functional materials. Interpretation of the structural design of thiourea based ligand and its incorporation into metal complexes can contribute to the understanding of preorganised self-assembly and open new pathways in design of novel soft materials. This work contributes to the unexplored library of hydrogen bonded metal complexes based on iridium. Further we examined the photoluminescence of the system of general formula [Ir(C^N)<sub>2</sub>(N^S)] and the effect of hydrogen bonding on the emission properties when combined with different <i>n</i>-heteroacenes.

Complementary Hydrogen Bonding and Block Copolymer Self-Assembly in Cooperation toward Stable Solar Cells with Tunable Morphologies

2013 ◽  
Vol 46 (22) ◽  
pp. 9021-9031 ◽  
Author(s):  
Fei Li ◽  
Kevin G. Yager ◽  
Noel M. Dawson ◽  
Jianzhong Yang ◽  
Kevin J. Malloy ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Solar Cells ◽  
Block Copolymer ◽  
Self Assembly

N-Tosyl-L-proline benzene hemisolvate: a rare example of a hydrogen-bonded carboxylic acid dimer with symmetrically disordered H atoms

2019 ◽  
Vol 75 (9) ◽  
pp. 1228-1233
Author(s):  
Joanna Wojnarska ◽  
Katarzyna Ostrowska ◽  
Marlena Gryl ◽  
Katarzyna Marta Stadnicka
Keyword(s):  
Hydrogen Bond ◽  
Carboxylic Acid ◽  
Self Assembly ◽  
Acid Group ◽  
Benzene Molecule ◽  
Noncovalent Interaction ◽  
Hydrogen Bond Donor ◽  
Donor And Acceptor ◽  
Carboxylic Acid Dimer ◽  
Hydrogen Bonded

The carboxylic acid group is an example of a functional group which possess a good hydrogen-bond donor (–OH) and acceptor (C=O). For this reason, carboxylic acids have a tendency to self-assembly by the formation of hydrogen bonds between the donor and acceptor sites. We present here the crystal structure of N-tosyl-L-proline (TPOH) benzene hemisolvate {systematic name: (2S)-1-[(4-methylbenzene)sulfonyl]pyrrolidine-2-carboxylic acid benzene hemisolvate}, C12H15NO4S·0.5C6H6, (I), in which a cyclic R 2 2(8) hydrogen-bonded carboxylic acid dimer with a strong O—(1 \over 2H)...(1 \over 2H)—O hydrogen bond is observed. The compound was characterized by single-crystal X-ray diffraction and NMR spectroscopy, and crystallizes in the space group I2 with half a benzene molecule and one TPOH molecule in the asymmetric unit. The H atom of the carboxyl OH group is disordered over a twofold axis. An analysis of the intermolecular interactions using the noncovalent interaction (NCI) index showed that the TPOH molecules form dimers due to the strong O—(1 \over 2H)...(1 \over 2H)—O hydrogen bond, while the packing of the benzene solvent molecules is governed by weak dispersive interactions. A search of the Cambridge Structural Database revealed that the disordered dimeric motif observed in (I) was found previously only in six crystal structures.

scholarly journals Straightforward preparation of supramolecular Janus nanorods by hydrogen bonding of end-functionalized polymers

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Shuaiyuan Han ◽  
Sandrine Pensec ◽  
Dijwar Yilmaz ◽  
Cédric Lorthioir ◽  
Jacques Jestin ◽  
...  
Keyword(s):  
Hydrogen Bonding ◽  
Self Assembly ◽  
Functional Materials ◽  
Phase Segregation ◽  
Building Blocks ◽  
Functionalized Polymers ◽  
Nanometer Range ◽  
One Dimensional ◽  
Oil In Water ◽  
Hydrogen Bonded

Abstract Janus cylinders are one-dimensional colloids that have two faces with different compositions and functionalities, and are useful as building blocks for advanced functional materials. Such anisotropic objects are difficult to prepare with nanometric dimensions. Here we describe a robust and versatile strategy to form micrometer long Janus nanorods with diameters in the 10-nanometer range, by self-assembly in water of end-functionalized polymers. The Janus topology is not a result of the phase segregation of incompatible polymer arms, but is driven by the interactions between unsymmetrical and complementary hydrogen bonded stickers. Therefore, even compatible polymers can be used to form these Janus objects. In fact, any polymers should qualify, as long as they do not prevent co-assembly of the stickers. To illustrate their applicative potential, we show that these Janus nanorods can efficiently stabilize oil-in-water emulsions.

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