“Release and catch” catalytic systems

Literature Information

Publication Date 2013-07-24
DOI 10.1039/C3GC41132J
Impact Factor 10.182
Authors

Michelangelo Gruttadauria, Francesco Giacalone, Renato Noto


View Original

Abstract

In this perspective article the “release and catch” catalytic system concept is discussed. A “release and catch” catalytic system is prepared by non-covalent immobilization of the catalytic moiety on a suitable support, but differently from the usual non-covalently supported catalyst, the catalytic moiety is released in solution over the course of the reaction and it is recaptured at the end of the reaction. Such a “catalyst-sponge like” or “boomerang” system allows one to combine the benefits of homogeneous and heterogeneous catalysis and can be applied to organometallic-based catalysts, organocatalysts and metal-based catalysts.

Related Literature

Quantitative analysis of 14N quadrupolar coupling using 1H detected 14N solid-state NMR

James A. Jarvis, Maria Concistre, Richard W. Bounds, Ilya Kuprov, Marina Carravetta, Philip T. F. Williamson

2019-02-27 Paper

DOI: 10.1039/C8CP06276E

Oxygen-functionalized TlTe buckled honeycomb from first-principles study

Qing Lu, Yi-Ming Wen, Zhao-Yi Zeng, Xiang-Rong Chen, Qi-Feng Chen

2019-02-12 Paper

DOI: 10.1039/C8CP07246A

Effect of an external electric field on capillary filling of water in hydrophilic silica nanochannels

Andres Rojano Crisson, Enrique Wagemann, Harvey A. Zambrano

2018-06-22 Paper

DOI: 10.1039/C8CP03186J

Electron localization in niobium doped CaMnO3 due to the energy difference of electronic states of Mn and Nb

Yi Li, Jian Liu, Ji-Chao Li, Yu-Fei Chen, Xin-Miao Zhang, Xue-Jin Wang, Fu-Ning Wang, Wen-Bin Su, Lan-Ling Zhao, Chun-Lei Wang

2018-07-23 Paper

DOI: 10.1039/C8CP02783H

Enhancing the electrocatalytic activity of 2H-WS2 for hydrogen evolution via defect engineering

Longfei Wu, Arno J. F. van Hoof, Nelson Y. Dzade, Lu Gao, Heiner Friedrich, Nora H. De Leeuw, Emiel J. M. Hensen, Jan P. Hofmann

2019-02-21 Paper

DOI: 10.1039/C9CP00722A

Time-resolved IR spectroscopy reveals mechanistic details of ion transport in the sodium pump Krokinobacter eikastus rhodopsin 2

Marvin Asido, Peter Eberhardt, Clara Nassrin Kriebel, Markus Braun, Clemens Glaubitz, Josef Wachtveitl

2019-02-01 Paper

DOI: 10.1039/C8CP07418F

Front cover

Cover

DOI: 10.1039/C8CP91831G

Insights on magnesium and sulfate ions’ adsorption on the surface of sodium alumino-silicate hydrate (NASH) gel: a molecular dynamics study

Yu Zhang, Tao Li, Dongshuai Hou, Jinglin Zhang, Jinyang Jiang

2018-06-19 Paper

DOI: 10.1039/C8CP02469C

Luminescence spectroscopy of oxazine dye cations isolated in vacuo

Christina Kjær, Steen Brøndsted Nielsen

2019-02-04 Paper

DOI: 10.1039/C8CP07340F

You might also like

Compound Q&A

What precautions should be taken when handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3)?

When handling 4-(2-Furylmethyl)thiomorpholine 1,1-dioxide (CAS: 79206-94-3), it ...

79206-94-34-(2-Furylmethyl)thi...
Compound Q&A

What precautions should be taken when handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9)?

When handling 4-Chloro-N-[2-(4-morpholinyl)ethyl]benzamide (CAS: 71320-77-9), it...

71320-77-94-Chloro-N-[2-(4-mor...
Compound Q&A

How should waste containing 2-[2-(2-Methoxyethoxy)ethoxy]ethyl 4-methylbenzenesulfonate (CAS: 62921-74-8) be handled?

Waste containing this compound (CAS: 62921-74-8) should be handled according to ...

62921-74-82-[2-(2-Methoxyethox...
Compound Q&A

How should waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate be handled?

Waste containing (S)-Methyl 2-amino-3-cyclohexylpropanoate should be collected i...

40056-18-6(S)-Methyl 2-amino-3...
166882-70-85-({4-[(2S,4R)-4-Hyd...
Compound Q&A

Are there alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid (CAS: 7312-27-8) in synthesis?

There are several alternatives to (2E)-3-(3,4-Dichlorophenyl)acrylic acid in syn...

7312-27-8(2E)-3-(3,4-Dichloro...
Compound Q&A

How should Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84-9) be stored?

Ethyl 6-(2-nitrophenyl)imidazo[2,1-b][1,3]thiazole-3-carboxylate (CAS: 925437-84...

925437-84-9Ethyl 6-(2-nitrophen...
Compound Q&A

How should waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) be handled?

Waste containing 2-(1,3-Thiazol-2-yl)ethanamine (CAS: 18453-07-1) should be coll...

18453-07-12-(1,3-Thiazol-2-yl)...
Compound Q&A

How is Methyl 5-iodo-2-methylbenzoate (CAS: 103440-54-6) typically synthesized?

Methyl 5-iodo-2-methylbenzoate can be synthesized through the iodination of meth...

103440-54-6Methyl 5-iodo-2-meth...
Compound Q&A

How is 5-Chloro[1,2,4]triazolo[1,5-a]pyridine (CAS: 1427399-34-5) typically synthesized?

5-Chloro[1,2,4]triazolo[1,5-a]pyridine is commonly synthesized via the condensat...

1427399-34-55-Chloro[1,2,4]triaz...

Source Journal

Green Chemistry

Green Chemistry
CiteScore: 16.1
Self-citation Rate: 7.5%
Articles per Year: 944

Green Chemistry provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on, but not limited to, the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998). Green chemistry is the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry is at the frontiers of this continuously-evolving interdisciplinary science and publishes research that attempts to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. Submissions on all aspects of research relating to the endeavour are welcome. The journal publishes original and significant cutting-edge research that is likely to be of wide general appeal. To be published, work must present a significant advance in green chemistry. Papers must contain a comparison with existing methods and demonstrate advantages over those methods before publication can be considered. For more information please see this Editorial. Coverage includes the following, but is not limited to: Design (e.g. biomimicry, design for degradation/recycling/reduced toxicity…) Reagents & Feedstocks (e.g. renewables, CO2, solvents, auxiliary agents, waste utilization…) Synthesis (e.g. organic, inorganic, synthetic biology…) Catalysis (e.g. homogeneous, heterogeneous, enzyme, whole cell…) Process (e.g. process design, intensification, separations, recycling, efficiency…) Energy (e.g. renewable energy, fuels, photovoltaics, fuel cells, energy storage, energy carriers…) Applications (e.g. electronics, dyes, consumer products, coatings, pharmaceuticals, preservatives, building materials, chemicals for industry/agriculture/mining…) Impact (e.g. safety, metrics, LCA, sustainability, (eco)toxicology…) Green chemistry is, by definition, a continuously-evolving frontier. Therefore, the inclusion of a particular material or technology does not, of itself, guarantee that a paper is suitable for the journal. To be suitable, the novel advance should have the potential for reduced environmental impact relative to the state of the art. Green Chemistry does not normally deal with research associated with 'end-of-pipe' or remediation issues.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.