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THE HUMAN RIGHTS MOVEMENT AND ITS RELATIONSHIP TO SOCIAL PROGRESS IS EXPLORED IN THIS ARTICLE. COMMUNIST PARTY POSITIONS ARE DESCRIBED, GIVEN THE LEVEL OF OPPRESSION WHICH EXISTS IN THEIR COUNTRIES, IN SPITE OF OFFICIAL PROCLOMATIONS TO THE CONTRARY. THE ORGANIZATION OF PUBLIC SUPPORT IN COUNTRIES AROUND THE WORLD IS CITED. SOCIAL STRUCTURE IS HELD ACCOUNTABLE FOR THE LACK OF PROGRESS, ACCORDING TO THE AUTHOR. EVEN GIVEN THIS, THE AUTHOR FEELS THAT A SOCIALIST SOCIETY IS BEST EQUIPPED TO DEAL WITH THE NECESSARY FREEDOMS AND ADJUST ACCORDINGLY.

[EN] Zirconium terephthalate UiO-66 type metal organic frameworks (MOFs) are known to be highly active, stable and reusable catalysts for the esterification of carboxylic acids with alcohols. Moreover, when defects are present in the structure of these MOFs, coordinatively unsaturated Zr ions with Lewis acid properties are created, which increase the catalytic activity of the resulting defective solids. In the present work, molecular modeling techniques combined with new experimental data on various defective hydrated and dehydrated materials allow to unravel the nature and role of defective active sites in the Fischer esterification and the role of coordinated water molecules to provide additional Bronsted sites. Periodic models of UiO-66 and UiO-66-NH2 catalysts have been used to unravel the reaction mechanism on hydrated and dehydrated materials. Various adsorption modes of water and methanol are investigated. The proposed mechanisms are in line with experimental observations that amino groups yield a reduction in the reaction barriers, although they have a passive role in modulating the electronic structure of the material. Water has a beneficial role on the reaction cycle by providing extra Bronsted sites and by providing stabilization for various intermediates through hydrogen bonds. (C) 2017 The Authors. Published by Elsevier Inc. ; This work is supported by the Fund for Scientific Research Flanders (FWO) (project number 3G048612), the Research Board of Ghent University (BOF) and BELSPO in the frame of IAP/7/05. This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 641887 (project acronym: DEFNET). Funding was also received from the European Union's Horizon 2020 research and innovation programme [consolidator ERC grant agreement no. 647755-DYNPOR (2015-2020)]. Computational resources (Stevin Supercomputer Infrastructure) and services were provided by Ghent University. Financial support from the ...

401 414 352 ; S ; [EN] Zirconium terephthalate UiO-66 type metal organic frameworks (MOFs) are known to be highly active, stable and reusable catalysts for the esterification of carboxylic acids with alcohols. Moreover, when defects are present in the structure of these MOFs, coordinatively unsaturated Zr ions with Lewis acid properties are created, which increase the catalytic activity of the resulting defective solids. In the present work, molecular modeling techniques combined with new experimental data on various defective hydrated and dehydrated materials allow to unravel the nature and role of defective active sites in the Fischer esterification and the role of coordinated water molecules to provide additional Bronsted sites. Periodic models of UiO-66 and UiO-66-NH2 catalysts have been used to unravel the reaction mechanism on hydrated and dehydrated materials. Various adsorption modes of water and methanol are investigated. The proposed mechanisms are in line with experimental observations that amino groups yield a reduction in the reaction barriers, although they have a passive role in modulating the electronic structure of the material. Water has a beneficial role on the reaction cycle by providing extra Bronsted sites and by providing stabilization for various intermediates through hydrogen bonds. (C) 2017 The Authors. Published by Elsevier Inc. This work is supported by the Fund for Scientific Research Flanders (FWO) (project number 3G048612), the Research Board of Ghent University (BOF) and BELSPO in the frame of IAP/7/05. This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No. 641887 (project acronym: DEFNET). Funding was also received from the European Union's Horizon 2020 research and innovation programme [consolidator ERC grant agreement no. 647755-DYNPOR (2015-2020)]. Computational resources (Stevin Supercomputer Infrastructure) and services were provided by Ghent University. Financial support ...

[EN] Heterogeneous single-site catalysts consist of isolated, well-defined, active sites that are spatially separated in a given solid and, ideally, structurally identical. In this review, the potential of metal-organic frameworks (MOFs) and covalent organic frameworks (COFs) as platforms for the development of heterogeneous single-site catalysts is reviewed thoroughly. In the first part of this article, synthetic strategies and progress in the implementation of such sites in these two classes of materials are discussed. Because these solids are excellent playgrounds to allow a better understanding of catalytic functions, we highlight the most important recent advances in the modelling and spectroscopic characterization of single-site catalysts based on these materials. Finally, we discuss the potential of MOFs as materials in which several single-site catalytic functions can be combined within one framework along with their potential as powerful enzyme-mimicking materials. The review is wrapped up with our personal vision on future research directions. ; S. M. J. Rogge, J. Hajek, and V. Van Speybroeck acknowledge the Fund for Scientific Research - Flanders (FWO), the Research Board of Ghent University (BOF) and BELSPO in the frame of IAP/7/05 for financial support. V. Van Speybroeck acknowledges funding from the European Union's Horizon 2020 research and innovation programme (consolidator ERC grant agreement no. 647755 - DYNPOR (2015-2020)). This project has received funding from the European Union's Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement no. 641887 (project acronym: DEFNET). W. Dewitte and C. Caratelli are acknowledged for technical support with the figures. J. Gascon acknowledges funding from the European Union's 2020 research and innovation programme (ERC grant agreement no. 335746 - CrystEng-MOF-MMM) and from the Dutch Organization for Scientific Research (NWO, VIDI grant agreement 723.012.107 - MetMOFCat). ; Rogge, SMJ.; Bavykina, A.; Hajek, J.; ...