Eduardo Vilaplana‐Ortego
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Research Subjects
Eduardo Vilaplana‐Ortego has a total of 20 co-authors. Here are the top co-authors by number of shared publications:
- Agustín Bueno-López
Department of Inorganic Chemistry—Faculty of Science University of Alicante 03690 Sant Vicent del Raspeig, Alicante Spain
2 shared publications - Alberto Fernández‐Alarcón
Institute of Molecular Science University of Valencia Catedrático José Beltrán 2 46980 Paterna Spain
2 shared publications - David Curiel
Department of Organic Chemistry – Faculty of Chemistry, University of Murcia, Murcia 30100, Spain
2 shared publications - Delia Bautista
Scientific Instrumentation Services University of Murcia 30100- Murcia Spain
2 shared publications - Enrique Ortí
Instituto de Ciencia Molecular (ICMol), Universitat de València , Paterna 46980
2 shared publications - Ion Such Basáñez
Technical Research Services (SSTTI) University of Alicante Parque Científico 03690 Sant Vicent del Raspeig, Alicante Spain
2 shared publications
Latest Publications
- Open Access
- 18 October 2024
- Published by Wiley in Angewandte Chemie
- Vol. 137 (1)
Rational Design of 7‐Azaindole‐Based Robust Microporous Hydrogen‐Bonded Organic Framework for Gas Sorption
7‐Azaindole has been integrated as building block with complementary N−H⋅⋅⋅N hydrogen bonding sites for the synthesis of a tetrahedral molecular tecton, namely tetra(α‐carbolin‐6‐yl)methane, TACM. The self‐assembly of this molecule results in a 3D hydrogen‐bonded organic framework (HOF). This supramolecular structure constitutes a crystalline microporous material with an extraordinary thermal and chemical robustness. Single crystal X‐ray diffraction reveals how the five‐fold catenation of diamonoid systems, stabilized by hydrogen bonds and π–π interactions, form an interpenetrated network with monodimensional channels. The structural features of the crystalline material are also observed by transmission electron microscopy (TEM). Additionally, the microporosity of the activated TACM‐HOF is characterized by gas sorption (N2, CO2, CH4 and H2) experiments performed at different pressures. A selective adsorption is observed for CO2 uptake and TACM‐HOF also presents a good adsorption capacity for H2 among supramolecular organic frameworks.
- 18 October 2024
- Published by Wiley in Angewandte Chemie
- Vol. 137 (1)
Open AccessRational Design of 7‐Azaindole‐Based Robust Microporous Hydrogen‐Bonded Organic Framework for Gas Sorption
7‐Azaindole has been integrated as building block with complementary N−H⋅⋅⋅N hydrogen bonding sites for the synthesis of a tetrahedral molecular tecton, namely tetra(α‐carbolin‐6‐yl)methane, TACM. The self‐assembly of this molecule results in a 3D hydrogen‐bonded organic framework (HOF). This supramolecular structure constitutes a crystalline microporous material with an extraordinary thermal and chemical robustness. Single crystal X‐ray diffraction reveals how the five‐fold catenation of diamonoid systems, stabilized by hydrogen bonds and π–π interactions, form an interpenetrated network with monodimensional channels. The structural features of the crystalline material are also observed by transmission electron microscopy (TEM). Additionally, the microporosity of the activated TACM‐HOF is characterized by gas sorption (N2, CO2, CH4 and H2) experiments performed at different pressures. A selective adsorption is observed for CO2 uptake and TACM‐HOF also presents a good adsorption capacity for H2 among supramolecular organic frameworks.
- Open Access
- 18 October 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 64 (1) , e202412981
Rational Design of 7‐Azaindole‐Based Robust Microporous Hydrogen‐Bonded Organic Framework for Gas Sorption
7‐Azaindole has been integrated as building block with complementary N−H⋅⋅⋅N hydrogen bonding sites for the synthesis of a tetrahedral molecular tecton, namely tetra(α‐carbolin‐6‐yl)methane, TACM. The self‐assembly of this molecule results in a 3D hydrogen‐bonded organic framework (HOF). This supramolecular structure constitutes a crystalline microporous material with an extraordinary thermal and chemical robustness. Single crystal X‐ray diffraction reveals how the five‐fold catenation of diamonoid systems, stabilized by hydrogen bonds and π–π interactions, form an interpenetrated network with monodimensional channels. The structural features of the crystalline material are also observed by transmission electron microscopy (TEM). Additionally, the microporosity of the activated TACM‐HOF is characterized by gas sorption (N2, CO2, CH4 and H2) experiments performed at different pressures. A selective adsorption is observed for CO2 uptake and TACM‐HOF also presents a good adsorption capacity for H2 among supramolecular organic frameworks.
- 18 October 2024
- Published by Wiley in Angewandte Chemie International Edition
- Vol. 64 (1) , e202412981
Open AccessRational Design of 7‐Azaindole‐Based Robust Microporous Hydrogen‐Bonded Organic Framework for Gas Sorption
7‐Azaindole has been integrated as building block with complementary N−H⋅⋅⋅N hydrogen bonding sites for the synthesis of a tetrahedral molecular tecton, namely tetra(α‐carbolin‐6‐yl)methane, TACM. The self‐assembly of this molecule results in a 3D hydrogen‐bonded organic framework (HOF). This supramolecular structure constitutes a crystalline microporous material with an extraordinary thermal and chemical robustness. Single crystal X‐ray diffraction reveals how the five‐fold catenation of diamonoid systems, stabilized by hydrogen bonds and π–π interactions, form an interpenetrated network with monodimensional channels. The structural features of the crystalline material are also observed by transmission electron microscopy (TEM). Additionally, the microporosity of the activated TACM‐HOF is characterized by gas sorption (N2, CO2, CH4 and H2) experiments performed at different pressures. A selective adsorption is observed for CO2 uptake and TACM‐HOF also presents a good adsorption capacity for H2 among supramolecular organic frameworks.