- Location
-
Deutsche Nationalbibliothek Frankfurt am Main
- Extent
-
Online-Ressource
- Language
-
Englisch
- Bibliographic citation
-
In: Physical Chemistry Chemical Physics 16.35 (2014): S. 18982-18992.
- Classification
-
Chemie
- Keyword
-
-
- Event
-
Veröffentlichung
- (where)
-
Erlangen
- (who)
-
Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
- (when)
-
2016
- Creator
-
Kellner, Ina D.
Nye, Leanne C.
Gernler, Marc Simon von
Li, Jing
Tzirakis, Manolis D.
Orfanopoulos, Michael
Drewello, Thomas
- URN
-
urn:nbn:de:bvb:29-opus4-76089
- Rights
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Last update
-
25.03.2025, 1:48 PM CET
Data provider
This object is provided by:
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Deutsche Nationalbibliothek. If you have any questions about the object, please contact the data provider.
Associated
- Kellner, Ina D.
- Nye, Leanne C.
- Gernler, Marc Simon von
- Li, Jing
- Tzirakis, Manolis D.
- Orfanopoulos, Michael
- Drewello, Thomas
- Friedrich-Alexander-Universität Erlangen-Nürnberg (FAU)
Time of origin
- 2016
Other Objects (12)
Crown ether-metalloporphyrins as ditopic receptors and pyropheophorbide-a conjugates for the photodynamic therapy of tumors
Conjugates of Tetraazamacrocycles and Crown Ethers, their Nickel and Cobalt Complexes and Reactivity towards Carbon Dioxide and Oxygen
Cooperative effects in multivalent crown ether/ammonium assemblies
Unveiling the nature of supramolecular crown ether–C60 interactions
Synthesis of Disila-Crown Ether Complexes and Heteroatomic Bridged Paracyclophanes
Synthesis of New Aza‐ and Thia‐Crown Ether Based Amino Acids
Synthesis of Multi-Porphyrin-Fullerene Conjugates as Models for Photosynthetic Light-Harvesting and Charge-Transfer Events
Fullerene
Ionic liquids, deep eutectic solvents, crown ethers, fluorinated solvents, glycols and glycerol
Rhodium‐catalyzed asymmetric macrocyclization towards crown ethers using hydroamination of Bis(allenes)
Fullerene : Technologieanalyse
Organotin containing crown ethers substituted ferrocene, ferrocenophanes for simultaneous complexation of cations and anions
Crown ether-metalloporphyrins as ditopic receptors and pyropheophorbide-a conjugates for the photodynamic therapy of tumors
Conjugates of Tetraazamacrocycles and Crown Ethers, their Nickel and Cobalt Complexes and Reactivity towards Carbon Dioxide and Oxygen
Cooperative effects in multivalent crown ether/ammonium assemblies
Unveiling the nature of supramolecular crown ether–C60 interactions
Synthesis of Disila-Crown Ether Complexes and Heteroatomic Bridged Paracyclophanes
Synthesis of New Aza‐ and Thia‐Crown Ether Based Amino Acids
Synthesis of Multi-Porphyrin-Fullerene Conjugates as Models for Photosynthetic Light-Harvesting and Charge-Transfer Events
Fullerene
Ionic liquids, deep eutectic solvents, crown ethers, fluorinated solvents, glycols and glycerol
Rhodium‐catalyzed asymmetric macrocyclization towards crown ethers using hydroamination of Bis(allenes)
Fullerene : Technologieanalyse
Organotin containing crown ethers substituted ferrocene, ferrocenophanes for simultaneous complexation of cations and anions
Crown ether-metalloporphyrins as ditopic receptors and pyropheophorbide-a conjugates for the photodynamic therapy of tumors
Conjugates of Tetraazamacrocycles and Crown Ethers, their Nickel and Cobalt Complexes and Reactivity towards Carbon Dioxide and Oxygen
Cooperative effects in multivalent crown ether/ammonium assemblies
Unveiling the nature of supramolecular crown ether–C60 interactions
Synthesis of Disila-Crown Ether Complexes and Heteroatomic Bridged Paracyclophanes
Synthesis of New Aza‐ and Thia‐Crown Ether Based Amino Acids
Synthesis of Multi-Porphyrin-Fullerene Conjugates as Models for Photosynthetic Light-Harvesting and Charge-Transfer Events
Fullerene
Ionic liquids, deep eutectic solvents, crown ethers, fluorinated solvents, glycols and glycerol
Rhodium‐catalyzed asymmetric macrocyclization towards crown ethers using hydroamination of Bis(allenes)
Fullerene : Technologieanalyse