Andreas Leng
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View article: Assessing the Relationship Between Pre-Operative Opioid Use and Outcomes of Patients with Cystic Fibrosis Undergoing Lung Transplantation
Assessing the Relationship Between Pre-Operative Opioid Use and Outcomes of Patients with Cystic Fibrosis Undergoing Lung Transplantation Open
View article: Au‐Catalyzed Energy Release in a Molecular Solar Thermal (MOST) System: A Combined Liquid‐Phase and Surface Science Study
Au‐Catalyzed Energy Release in a Molecular Solar Thermal (MOST) System: A Combined Liquid‐Phase and Surface Science Study Open
Molecular solar thermal systems (MOSTs) are molecular systems based on couples of photoisomers (photoswitches), which combine solar energy conversion, storage, and release. In this work, we address the catalytically triggered energy releas…
View article: Au catalyzed energy release in a molecular solar thermal (MOST) system: A combined liquid-phase and surface science study
Au catalyzed energy release in a molecular solar thermal (MOST) system: A combined liquid-phase and surface science study Open
Raw Data, evaluated files and a list of experiments is provided.
View article: Au catalyzed energy release in a molecular solar thermal (MOST) system: A combined liquid-phase and surface science study
Au catalyzed energy release in a molecular solar thermal (MOST) system: A combined liquid-phase and surface science study Open
Raw Data, evaluated files and a list of experiments is provided.
View article: Cover Feature: Surface Studies on the Energy Release of the MOST System 2‐Carbethoxy‐3‐Phenyl‐Norbornadiene/Quadricyclane (PENBD/PEQC) on Pt(111) and Ni(111) (Chem. Eur. J. 25/2023)
Cover Feature: Surface Studies on the Energy Release of the MOST System 2‐Carbethoxy‐3‐Phenyl‐Norbornadiene/Quadricyclane (PENBD/PEQC) on Pt(111) and Ni(111) (Chem. Eur. J. 25/2023) Open
The energy storage cycle of the molecular solar thermal (MOST) system has been investigated. In particular, upon irradiation, the energy-lean 2-carbethoxy-3-phenyl-norbornadiene is converted into its energy-rich quadricyclane isomer. The e…
View article: Surface Studies on the Energy Release of the MOST System 2‐Carbethoxy‐3‐Phenyl‐Norbornadiene/Quadricyclane (PENBD/PEQC) on Pt(111) and Ni(111)
Surface Studies on the Energy Release of the MOST System 2‐Carbethoxy‐3‐Phenyl‐Norbornadiene/Quadricyclane (PENBD/PEQC) on Pt(111) and Ni(111) Open
Novel energy‐storage solutions are necessary for the transition from fossil to renewable energy sources. Auspicious candidates are so‐called molecular solar thermal (MOST) systems. In our study, we investigate the surface chemistry of a de…
View article: Driving the quadricyclane-to-norbornadiene isomerization by charge separation with perylenediimide as electron acceptor
Driving the quadricyclane-to-norbornadiene isomerization by charge separation with perylenediimide as electron acceptor Open
The complementary use of time-resolved and steady-state spectroscopies has made it possible to describe the full reaction coordinate regarding the photoisomerization of NBDs featuring electron accepting PDIs.
View article: Front Cover: Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111) (ChemPhysChem 16/2022)
Front Cover: Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111) (ChemPhysChem 16/2022) Open
The Front Cover shows the concept of molecular solar thermal (MOST) energy storage systems, whereby the light-harvesting process is combined with storage as molecular strain. The photoinduced isomerization of 2,3-dicyano-norbornadiene to i…
View article: Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111)
Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111) Open
The front cover artwork is provided by the group of Prof. Dr. Christian Papp at Physical Chemistry II of FAU Erlangen‐Nürnberg and FU Berlin. The image shows the isomerization reaction of the molecule pair 2,3‐dicyano‐norbornadiene/quadric…
View article: Reversible Photoinduced Conversion of Unprecedented Norbornadiene‐Based Photoswitches with Redox‐Active Naphthalene Diimide Functionalities
Reversible Photoinduced Conversion of Unprecedented Norbornadiene‐Based Photoswitches with Redox‐Active Naphthalene Diimide Functionalities Open
An unprecedented compound class of functional organic hybrids consisting of a photoswitchable norbornadiene building block and a redoxactive chromophore, namely naphthalene diimide, were designed and synthesized. Within these structures th…
View article: Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111)
Surface Chemistry of the Molecular Solar Thermal Energy Storage System 2,3‐Dicyano‐Norbornadiene/Quadricyclane on Ni(111) Open
Molecular solar thermal (MOST) systems are a promising approach for the introduction of sustainable energy storage solutions. We investigated the feasibility of the dicyano‐substituted norbornadiene/quadricyclane molecule pair on Ni(111) f…
View article: Encapsulation of Hydrophobic Drugs in Shell-by-Shell Coated Nanoparticles for Radio—and Chemotherapy—An In Vitro Study
Encapsulation of Hydrophobic Drugs in Shell-by-Shell Coated Nanoparticles for Radio—and Chemotherapy—An In Vitro Study Open
Our research objective was to develop novel drug delivery vehicles consisting of TiO2 and Al2O3 nanoparticles encapsulated by a bilayer shell that allows the reversible embedment of hydrophobic drugs. The first shell is formed by covalent …