- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring ** ; day:12 ; month:08 ; year:2021 ; extent:9
Angewandte Chemie / International edition. International edition ; (12.08.2021) (gesamt 9)
- Creator
-
Casademont‐Reig, Irene
Guerrero‐Avilés, Raúl
Ramos‐Cordoba, Eloy
Torrent‐Sucarrat, Miquel
Matito, Eduard
- DOI
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10.1002/anie.202108997
- URN
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urn:nbn:de:101:1-2021081215181699954296
- Rights
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
14.08.2025, 10:45 AM CEST
Data provider
This object is provided by:
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Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Casademont‐Reig, Irene
- Guerrero‐Avilés, Raúl
- Ramos‐Cordoba, Eloy
- Torrent‐Sucarrat, Miquel
- Matito, Eduard
Other Objects (12)
How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring **
Aromatic C–H⋯π, C–H⋯O and parallel aromatic–aromatic interactions in the crystal structure of meso-tetrakis[4-(benzyloxy)phenyl]porphyrin
Conformational switching of ethano-bridged Cu,H2-bis-porphyrin induced by aromatic amines
Constructive quantum interference in a bis-copper six-porphyrin nanoring
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
A Nature‐Inspired Antioxidant Strategy based on Porphyrin for Aromatic Hydrocarbon Containing Fuel Cell Membranes **
Porphyrin-Isomere
Porphyrin-lipid nanovesicles (Porphysomes) are effective photosensitizers for photodynamic therapy
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Now we are six
How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring **
Aromatic C–H⋯π, C–H⋯O and parallel aromatic–aromatic interactions in the crystal structure of meso-tetrakis[4-(benzyloxy)phenyl]porphyrin
Conformational switching of ethano-bridged Cu,H2-bis-porphyrin induced by aromatic amines
Constructive quantum interference in a bis-copper six-porphyrin nanoring
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
A Nature‐Inspired Antioxidant Strategy based on Porphyrin for Aromatic Hydrocarbon Containing Fuel Cell Membranes **
Porphyrin-Isomere
Porphyrin-lipid nanovesicles (Porphysomes) are effective photosensitizers for photodynamic therapy
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Now we are six
How Aromatic Are Molecular Nanorings? The Case of a Six‐Porphyrin Nanoring **
Aromatic C–H⋯π, C–H⋯O and parallel aromatic–aromatic interactions in the crystal structure of meso-tetrakis[4-(benzyloxy)phenyl]porphyrin
Conformational switching of ethano-bridged Cu,H2-bis-porphyrin induced by aromatic amines
Constructive quantum interference in a bis-copper six-porphyrin nanoring
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
Porous Molecular Crystals Derived from Cofacial Porphyrin/Phthalocyanine Heterodimers
A Nature‐Inspired Antioxidant Strategy based on Porphyrin for Aromatic Hydrocarbon Containing Fuel Cell Membranes **
Porphyrin-Isomere
Porphyrin-lipid nanovesicles (Porphysomes) are effective photosensitizers for photodynamic therapy
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen
Supramolecular fullerene-porphyrin architectures : = Supramolekulare Fulleren-Porphyrin-Architekturen