Showing posts with label MESOPOROUS METAL–ORGANIC FRAMEWORKS. Show all posts
Showing posts with label MESOPOROUS METAL–ORGANIC FRAMEWORKS. Show all posts

Friday, August 29, 2014

Structural Diversities in Metal-Organic Coordination Polymers Based on Flexibility in Organic Spacer

CATEGORY: MESOPOROUS METAL–ORGANIC FRAMEWORKS 
Structural Diversities in Metal-Organic Coordination Polymers Based on Flexibility in Organic Spacer


Type
Journal Article
Author
Anindita Chakraborty
Author
Tapas Kumar Maji
URL
Volume
94
Issue
1
Pages
69-78
Publication
Journal of the Indian Institute of Science
Date
2014/01/01
Abstract
Metal-organic coordination polymers with their various novel structural motifs have drawn intense research interests over the last few decades. Interestingly, flexibility of the organic spacers in such metalorganic coordination polymers can direct various structural topology and intricate networks. A novel 1D coordination polymer and some other illustrative examples with different flexible ligands like 1,2-bis(4-pyridyl)ethane (bpe) and 1,3-bis(4-pyridyl)propane (bpp) have been discussed in this review.
Both gauche and anti-conformations could be adopted by the bpe ligand, and hence diverse structures can be furnished. Further flexibility could be achieved by exploiting longer ligand like 1,3-bis(4-pyridyl) propane (bpp). Our group has been pursuing research to furnish such flexible compounds and study their different functionalities. An account of design of such diverse systems by employing judicious ligand design strategy and their different structural aspects will be presented in this review.

Metal-organic frameworks based upon non-zeotype 4-connected topology

CATEGORY: MESOPOROUS METAL–ORGANIC FRAMEWORKS 
Metal-organic frameworks based upon non-zeotype 4-connected topology


Type
Journal Article
Author
Dong-Sheng Li
Author
Ya-Pan Wu
Author
Jun Zhao
Author
Jian Zhang
Author
Jack Y. Lu
URL
Volume
261
Pages
1-27
Publication
Coordination Chemistry Reviews
Date
February 15, 2014
Abstract
Understanding the basic correlations between the composition, physical properties and topology of the underlying nets is crucial to further design and successfully prepare for the functional metal-organic framework materials,. Authors focus on recent advances in metal-organic frameworks (MOFs) that possess more common non-zeotype 4-connected topological nets (such as sql, kag, nbo, lvt, cds, qtz, dia, lon, pts, etc.)
They discuss the synthetic strategies of non-zeotype 4-connected MOFs and their related properties. They emphasize how to establish basic design principles and synthetic methodology to construct the same topological MOFs with different functions using specifically designed organic linkers.

Highly mesoporous metal–organic framework assembled in a switchable solvent

CATEGORY: MESOPOROUS METAL–ORGANIC FRAMEWORKS 
Highly mesoporous metal–organic framework assembled in a switchable solvent


Type
Journal Article
Author
Li Peng
Author
Jianling Zhang
Author
Zhimin Xue
Author
Buxing Han
Author
Xinxin Sang
Author
Chengcheng Liu
Author
Guanying Yang
URL
Volume
5
Publication
Nature Communications
Date
July 22, 2014
Abstract
The mesoporous metal–organic frameworks are a family of materials that have pore sizes ranging from 2 to 50 nm, which have shown promising applications in catalysis, adsorption, chemical sensing and so on. The preparation of mesoporous metal–organic frameworks usually needs the supramolecular or cooperative template strategy. Here we report the template-free assembly of mesoporous metal–organic frameworks by using ​CO2-expanded liquids as switchable solvents.
The mesocellular metal–organic frameworks with large mesopores (13–23 nm) are formed, and their porosity properties can be easily adjusted by controlling ​CO2 pressure. Moreover, the use of ​CO2 can accelerate the reaction for metal–organic framework formation from metal salt and organic linker due to the viscosity-lowering effect of ​CO2, and the product can be recovered through ​CO2 extraction. The as-synthesized mesocellular metal–organic frameworks are highly active in catalysing the aerobic oxidation of benzylic alcohols under mild temperature at atmospheric pressure.