Cocrystallization of pyrogallol[4]arenes with target molecules

2011 ◽  
Author(s):  
◽  
Drew A. Fowler

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT REQUEST OF AUTHOR.] Supramolecular chemistry, in its simplest and broadest description, is the chemistry of intermolecular interactions or chemistry of the noncovalent bond. Supramolecular chemistry is rooted in discoveries, such as the chlorine clathrate found in 1810 by Sir Humphry Davy, and concepts, such as coordination chemistry (1893-Werner) and the lock-and-key concept (1894-Fischer). The broad definition of supramolecular chemistry can be applied to a vast subject range including naturally occurring assemblies, such as proteins and the double helix of DNA. Today, a key interest of supramolecular chemists is the design of functional multi-component systems constructed from smaller molecular building blocks. This research focuses specifically on the supramolecular chemistry of a family of macrocycles called calixarenes, specifically the pyrogallol derivatives pyrogallol[4]arenes. Due to the bowl-like shape of the macrocycles and the presence of 12 upper-rim hydroxyls, pyrogallol[4]arenes have been found to exhibit a number of interesting supramolecular properties. The following dissertation contains the description of advances that have been made using these macrocycles. This work illustrates the expansion of a project dealing with the cocrystallization, and encapsulation of fluorescent reporter molecules with a variety of pyrogallol[4]arenes in different solvent systems. The description of a number of crystal structures that is offered will illustrate how, through thoughtful experimentation, the successful design of a new host molecular capsule was carried out and broadened to include a number of guest molecules. The target molecules have also been expanded from the fluorescent reporters to a variety of possible targets molecules. The solid-state structures discussed include multiple cocrystals of gabapentin, an active pharmaceutical ingredient, and structures containing the organometallic sandwich complex ferrocene.

2009 ◽  
Vol 13 (04n05) ◽  
pp. 461-470 ◽  
Author(s):  
Joaquim Crusats ◽  
Zoubir El-Hachemi ◽  
Carlos Escudero ◽  
Josep M. Ribó

The formation and structure of the title aggregates are paradigms of the self-assembly of amphiphilic molecular building blocks in supramolecular chemistry. This review summarizes the research in the University of Barcelona on the homoassociation of the water soluble meso 4-sulfonatophenyl-and phenyl substituted porphyrins.


2014 ◽  
Vol 16 (22) ◽  
pp. 10388-10397 ◽  
Author(s):  
Takeshi Ueki ◽  
Ryo Yoshida

Herein, we summarise the recent developments in self-oscillating polymeric materials based on the concepts of supramolecular chemistry, where aggregates of molecular building blocks with non-covalent bonds evolve the temporal or spatiotemporal structure.


Organics ◽  
2021 ◽  
Vol 2 (3) ◽  
pp. 161-273
Author(s):  
Daisuke Sato ◽  
Zhiyuan Wu ◽  
Hikaru Fujita ◽  
Jonathan S. Lindsey

A growing theme in chemistry is the joining of multiple organic molecular building blocks to create functional molecules. Diverse derivatizable structures—here termed “scaffolds” comprised of “hubs”—provide the foundation for systematic covalent organization of a rich variety of building blocks. This review encompasses 30 tri- or tetra-armed molecular hubs (e.g., triazine, lysine, arenes, dyes) that are used directly or in combination to give linear, cyclic, or branched scaffolds. Each scaffold is categorized by graph theory into one of 31 trees to express the molecular connectivity and overall architecture. Rational chemistry with exacting numbers of derivatizable sites is emphasized. The incorporation of water-solubilization motifs, robust or self-immolative linkers, enzymatically cleavable groups and functional appendages affords immense (and often late-stage) diversification of the scaffolds. Altogether, 107 target molecules are reviewed along with 19 syntheses to illustrate the distinctive chemistries for creating and derivatizing scaffolds. The review covers the history of the field up through 2020, briefly touching on statistically derivatized carriers employed in immunology as counterpoints to the rationally assembled and derivatized scaffolds here, although most citations are from the past two decades. The scaffolds are used widely in fields ranging from pure chemistry to artificial photosynthesis and biomedical sciences.


Catalysts ◽  
2019 ◽  
Vol 9 (2) ◽  
pp. 163 ◽  
Author(s):  
Loïc Leclercq ◽  
Grégory Douyère ◽  
Véronique Nardello-Rataj

The directed assembly of molecular building blocks into discrete supermolecules or extended supramolecular networks through noncovalent intermolecular interactions is an ongoing challenge in chemistry. This challenge may be overcome by establishing a hierarchy of intermolecular interactions that, in turn, may facilitate the edification of supramolecular assemblies. As noncovalent interactions can be used to accelerate the reaction rates and/or to increase their selectivity, the development of efficient and practical catalytic systems, using supramolecular chemistry, has been achieved during the last few decades. However, between discrete and extended supramolecular assemblies, the newly developed “colloidal tectonics” concept allows us to link the molecular and macroscopic scales through the structured engineering of colloidal structures that can be applied to the design of predictable, versatile, and switchable catalytic systems. The main cutting-edge strategies involving supramolecular chemistry and self-organization in catalysis will be discussed and compared in this review.


Author(s):  
Daniel Lambrecht ◽  
Eric Berquist

We present a first principles approach for decomposing molecular linear response properties into orthogonal (additive) plus non-orthogonal/cooperative contributions. This approach enables one to 1) identify the contributions of molecular building blocks like functional groups or monomer units to a given response property and 2) quantify cooperativity between these contributions. In analogy to the self consistent field method for molecular interactions, SCF(MI), we term our approach LR(MI). The theory, implementation and pilot data are described in detail in the manuscript and supporting information.


Polyhedron ◽  
2011 ◽  
Vol 30 (15) ◽  
pp. 2550-2557 ◽  
Author(s):  
Katarzyna Suracka ◽  
Alina Bieńko ◽  
Jerzy Mroziński ◽  
Rafał Kruszyński ◽  
Dariusz Bieńko ◽  
...  

2021 ◽  
Author(s):  
Luuk Kortekaas ◽  
Julian Simke ◽  
Niklas Arndt ◽  
Marcus Böckmann ◽  
Nikos Doltsinis ◽  
...  

Molecular photoswitches play a vital role in the development of responsive materials. These molecular building blocks are particularly attractive when multiple stimuli can be combined to bring about physical changes,...


2015 ◽  
Vol 03 (01n02) ◽  
pp. 1540004 ◽  
Author(s):  
Xialu Wu ◽  
David J. Young ◽  
T. S. Andy Hor

As molecular synthesis advances, we are beginning to learn control of not only the chemical reactivity (and function) of molecules, but also of their interactions with other molecules. It is this basic idea that has led to the current explosion of supramolecular science and engineering. Parallel to this development, chemists have been actively pursuing the design of very large molecules using basic molecular building blocks. Herein, we review the general development of supramolecular chemistry and particularly of two new branches: supramolecular coordination complexes (SCCs) and metal organic frameworks (MOFs). These two fields are discussed in detail with typical examples to illustrate what is now possible and what challenges lie ahead for tomorrow's molecular artisans.


2008 ◽  
pp. 4436 ◽  
Author(s):  
Christian Schenk ◽  
Florian Henke ◽  
Gustavo Santiso-Quiñones ◽  
Ingo Krossing ◽  
Andreas Schnepf

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