Importance of Molecular-Level Contacts under Solventless Conditions for Chemical Reactions and Self-Assembly

2007 ◽  
Vol 80 (8) ◽  
pp. 1617-1623 ◽  
Author(s):  
Akihiro Orita ◽  
Junji Okano ◽  
Genta Uehara ◽  
Lasheng Jiang ◽  
Junzo Otera
Author(s):  
Peter Atkins

Illustrated with remarkable new full-color images--indeed, one or more on every page--and written by one of the world's leading authorities on the subject, Reactions offers a compact, pain-free tour of the inner workings of chemistry. Reactions begins with the chemical formula almost everyone knows--the formula for water, H2O--a molecule with an "almost laughably simple chemical composition." But Atkins shows that water is also rather miraculous--it is the only substance whose solid form is less dense than its liquid (hence ice floats in water)--and incredibly central to many chemical reactions, as it is an excellent solvent, being able to dissolve gases and many solids. Moreover, Atkins tells us that water is actually chemically aggressive, and can react with and destroy the compounds dissolved in it, and he shows us what happens at the molecular level when water turns to ice--and when it melts. Moving beyond water, Atkins slowly builds up a toolkit of basic chemical processes, including precipitation (perhaps the simplest of all chemical reactions), combustion, reduction, corrosion, electrolysis, and catalysis. He then shows how these fundamental tools can be brought together in more complex processes such as photosynthesis, radical polymerization, vision, enzyme control, and synthesis. Peter Atkins is the world-renowned author of numerous best-selling chemistry textbooks for students. In this crystal-clear, attractively illustrated, and insightful volume, he provides a fantastic introductory tour--in just a few hundred colorful and lively pages - for anyone with a passing or serious interest in chemistry.


2021 ◽  
Vol 16 (1) ◽  
Author(s):  
Chunzheng Lv ◽  
Lirong He ◽  
Jiahong Tang ◽  
Feng Yang ◽  
Chuhong Zhang

AbstractAs an important photoconductive hybrid material, perylene/ZnO has attracted tremendous attention for photovoltaic-related applications, but generally faces a great challenge to design molecular level dispersed perylenes/ZnO nanohybrids due to easy phase separation between perylenes and ZnO nanocrystals. In this work, we reported an in-situ reaction method to prepare molecular level dispersed H-aggregates of perylene bisimide/ZnO nanorod hybrids. Surface photovoltage and electric field-induced surface photovoltage spectrum show that the photovoltage intensities of nanorod hybrids increased dramatically for 100 times compared with that of pristine perylene bisimide. The enhancement of photovoltage intensities resulting from two aspects: (1) the photo-generated electrons transfer from perylene bisimide to ZnO nanorod due to the electric field formed on the interface of perylene bisimide/ZnO; (2) the H-aggregates of perylene bisimide in ZnO nanorod composites, which is beneficial for photo-generated charge separation and transportation. The introduction of ordered self-assembly thiol-functionalized perylene-3,4,9,10-tetracarboxylic diimide (T-PTCDI)/ ZnO nanorod composites induces a significant improvement in incident photo-to-electron conversion efficiency. This work provides a novel mentality to boost photo-induced charge transfer efficiency, which brings new inspiration for the preparation of the highly efficient solar cell.


2014 ◽  
Vol 43 (5) ◽  
pp. 1387-1399 ◽  
Author(s):  
Xianjue Chen ◽  
Nicole M. Smith ◽  
K. Swaminathan Iyer ◽  
Colin L. Raston

2020 ◽  
Vol 10 (11) ◽  
pp. 3987-3998 ◽  
Author(s):  
Sweta Sharma ◽  
Ibrahim E. Awad ◽  
Arpita Yadav ◽  
Raymond A. Poirier

Nanomaterials ◽  
2020 ◽  
Vol 10 (5) ◽  
pp. 1008 ◽  
Author(s):  
Ximena Zottig ◽  
Mélanie Côté-Cyr ◽  
Dominic Arpin ◽  
Denis Archambault ◽  
Steve Bourgault

Life-inspired protein supramolecular assemblies have recently attracted considerable attention for the development of next-generation vaccines to fight against infectious diseases, as well as autoimmune diseases and cancer. Protein self-assembly enables atomic scale precision over the final architecture, with a remarkable diversity of structures and functionalities. Self-assembling protein nanovaccines are associated with numerous advantages, including biocompatibility, stability, molecular specificity and multivalency. Owing to their nanoscale size, proteinaceous nature, symmetrical organization and repetitive antigen display, protein assemblies closely mimic most invading pathogens, serving as danger signals for the immune system. Elucidating how the structural and physicochemical properties of the assemblies modulate the potency and the polarization of the immune responses is critical for bottom-up design of vaccines. In this context, this review briefly covers the fundamentals of supramolecular interactions involved in protein self-assembly and presents the strategies to design and functionalize these assemblies. Examples of advanced nanovaccines are presented, and properties of protein supramolecular structures enabling modulation of the immune responses are discussed. Combining the understanding of the self-assembly process at the molecular level with knowledge regarding the activation of the innate and adaptive immune responses will support the design of safe and effective nanovaccines.


1997 ◽  
Vol 62 (4) ◽  
pp. 527-557 ◽  
Author(s):  
Martin Bělohradský ◽  
Françisco M. Raymo ◽  
J. Fraser Stoddart

The art and science of introducing mechanical-interlocking at the molecular level in order to generate catenanes - molecules composed of two or more macrocyclic components - offers the opportunity of constructing a new range of molecular compounds possessing intriguing properties. However, the topological features displayed by catenanes has rendered the syntheses of such molecular compounds an extremely challenging task for synthetic chemists to address. Their early syntheses were based upon either statistical approaches - the threading of a small amount of a macrocycle on to an acyclic precursor as a chance event - or directed approaches, relying upon the temporary introduction of covalent bonds in the multistep synthesis of a so-called precatenane, followed by its conversion ultimately into a catenane. These approaches afforded catenanes in very low yields overall and only after following tedious and laborious synthetic procedures. Fortunately, however, with the advent of supramolecular chemistry, template-directed methods that allow us to self-assemble [n]catenanes much more efficiently have become available. Numerous successful template-directed syntheses have now emerged - some by chance and others by design. These methods have been based upon (i) metal coordinating, (ii) hydrogen bonding, (iii) solvophobic, and/or (iv) π-π stacking interactions which have been found to govern self-assembly processes to catenated compounds from appropriate precursors. Their relative simplicity, the high degree of control with which they can be employed, and the remarkable efficiency with which they proceed has already provided the opportunity to synthetic chemists to self-assemble a series of [n]catenanes, incorporating from two up to five mechanically-interlocked macrocyclic components.


2015 ◽  
Vol 16 (12) ◽  
pp. 10797-10820 ◽  
Author(s):  
Dnyaneshwar Rasale ◽  
Apurba Das

2017 ◽  
Vol 41 (2) ◽  
pp. 639-649 ◽  
Author(s):  
Raffaella Lettieri ◽  
Lenka Cardová ◽  
Emanuela Gatto ◽  
Claudia Mazzuca ◽  
Donato Monti ◽  
...  

Transfer of chiral information from the molecular level to the mesoscale has been obtained by hierarchical self-assembly of tetrasteroid-porphyrins.


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