Recent developments in dipyrrin based metal complexes: Self-assembled nanoarchitectures and materials applications

2020 ◽  
Vol 24 (05n07) ◽  
pp. 646-661
Author(s):  
Qian Jiang ◽  
Nicolas Desbois ◽  
Shifa Wang ◽  
Claude P. Gros

While dipyrrin-boron complexes (BODIPYs) and their derivatives have attracted much attention, dipyrrin-based metal complexes recently appeared as a novel luminescent material. So far, dipyrrin-metal complexes have been regarded as non-luminescent or weakly luminescent. Interestingly, introduction of steric hindrance at the meso-position and the development of heteroleptic complexes with proper frontier orbital ordering are two recent strategies that have been developed to improve their luminescent ability. Compared with BODIPYs, one of the distinctive advantages of dipyrrin-metal complexes is that they can form a series of self-assembled supramolecules and polymer assemblies via facile coordination reactions. In recent times, several supramolecular, coordination polymers and Metal-Organic Frameworks (MOFs) have been developed, [Formula: see text] by spontaneous coordination reactions between dipyrrin ligands and metal ions. As a novel luminescent material, dipyrrin-metal complexes have been applied in many fields. This review article summarizes recent developments in dipyrrin-metal complexes from the viewpoint of the improvement of luminescent ability, the formation of supramolecular and coordination polymers and their potential applications.

Author(s):  
Ayushi Singh ◽  
Ashish Kumar Singh ◽  
Jian-Qiang Liu ◽  
Abhinav Kumar

Metal-organic frameworks (MOFs) or coordination polymers (CPs) are regarded as new variety of materials that find potential applications in plethora of areas such as gas/small molecule absorption/separation, gas storage, membranes...


Author(s):  
Ryuichi Murase ◽  
Bowen Ding ◽  
Qinyi Gu ◽  
Deanna M. D'Alessandro

Electroactive and conducting framework materials, encompassing coordination polymers and metal–organic frameworks, have captured the imagination of the scientific community owing to their highly designable nanoporous structures and their potential applications in electrochromic devices, electrocatalysts, porous conductors, batteries and solar energy harvesting systems, among many others. While they are now considered integral members of the broader field of inorganic materials, it is timely to reflect upon their strengths and challenges compared with ‘traditional’ solid-state materials such as minerals, pigments and zeolites. Indeed, the latter have been known since ancient times and have been prized for centuries in fields as diverse as art, archaeology and industrial catalysis. This opinion piece considers a brief historical perspective of traditional electroactive and conducting inorganic materials, with a view towards very recent experimental progress and new directions for future progress in the burgeoning area of coordination polymers and metal–organic frameworks. Overall, this article bears testament to the rich history of electroactive solids and looks at the challenges inspiring a new generation of scientists. This article is part of the theme issue ‘Mineralomimesis: natural and synthetic frameworks in science and technology’.


Inorganics ◽  
2021 ◽  
Vol 9 (11) ◽  
pp. 81
Author(s):  
Alessia Tombesi ◽  
Claudio Pettinari

Metal–organic frameworks (MOFs) are a family of porous crystalline materials that serve in some cases as versatile platforms for catalysis. In this review, we overview the recent developments about the use of these species as heterogeneous catalysts in olefin epoxidation and carbon dioxide cycloaddition. We report the most important results obtained in this field relating them to the presence of specific organic linkers, metal nodes or clusters and mixed-metal species. Recent advances obtained with MOF nanocomposites were also described. Finally we compare the results and summarize the major insights in specific Tables, outlining the major challenges for this emerging field. This work could promote new research aimed at producing coordination polymers and MOFs able to catalyse a broader range of CO2 consuming reactions.


2007 ◽  
Vol 79 (12) ◽  
pp. 2155-2177 ◽  
Author(s):  
Tapas Kumar Maji ◽  
Susumu Kitagawa

Remarkable advances in the recent development of porous compounds based upon coordination polymers have paved the way toward functional chemistry having potential applications such as gas storage, separation, and catalysis. From the synthetic point of view, the advantage is a designable framework, which can readily be constructed from building blocks, the so-called bottom-up assembly. Compared with conventional porous materials such as zeolites and activated carbons, porous inorganic-organic hybrid frameworks have higher potential for adsorption of small molecules because of their designability with respect to the coordination geometry around the central metal ion as well as size and probable multifunctionality of bridging organic ligands. Although rigidity and robustness of porous framework with different degree of adsorption are the most studied properties of metal-organic coordination frameworks, there are few studies on dynamic porous frameworks, which could open up a new dimension in materials chemistry.


2015 ◽  
Vol 51 (24) ◽  
pp. 5077-5080 ◽  
Author(s):  
Valentina Brega ◽  
Matthias Zeller ◽  
Yufan He ◽  
H. Peter Lu ◽  
Jeremy K. Klosterman

Multi-responsive metal–organic cages bearing internal amines groups formed 1D supramolecular coordination polymers or covalent host–guest complexes from solutions of pre-assembled cages.


2020 ◽  
Vol 56 (85) ◽  
pp. 12969-12972
Author(s):  
Matthew L. Schneider ◽  
Oliver M. Linder-Patton ◽  
Witold M. Bloch

A covalent deprotection strategy facilitates the self-polymerisation of amine-functionalised Cu4L4 metal–organic cages into supramolecular coordination polymers with tunable porosity.


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