ABSTRACT
An amphiphilic Ru-containing block copolymer is used as a photoactivated polymetallodrug for anticancer phototherapy. The block copolymer self-assembles into nanoparticles, which can accumulate at tumor sites in a mouse model. Red light irradiation of the block copolymer nanoparticles releases anticancer Ru complexes and generates cytotoxic 1 O2 , both of which can inhibit tumor growth.
Subject(s)
Ruthenium/chemistry , Animals , Light , Mice , Neoplasms , Photochemotherapy , Photosensitizing Agents , PhototherapyABSTRACT
The storage of electric energy is of ever growing importance for our modern, technology-based society, and novel battery systems are in the focus of research. The substitution of conventional metals as redox-active material by organic materials offers a promising alternative for the next generation of rechargeable batteries since these organic batteries are excelling in charging speed and cycling stability. This review provides a comprehensive overview of these systems and discusses the numerous classes of organic, polymer-based active materials as well as auxiliary components of the battery, like additives or electrolytes. Moreover, a definition of important cell characteristics and an introduction to selected characterization techniques is provided, completed by the discussion of potential socio-economic impacts.
ABSTRACT
Redox-active polymers have received recently significant interest as active materials in secondary organic batteries. We designed a redox-active monomer, namely 2-vinyl-4,8-dihydrobenzo[1,2-b:4,5-b']dithiophene-4,8-dione that exhibits two one-electron redox reactions and has a low molar mass, resulting in a high theoretical capacity of 217 mAh/g. The free radical polymerization of the monomer was optimized by variation of solvent and initiator. The electrochemical behavior of the obtained polymer was investigated using cyclic voltammetry. The utilization of lithium salts in the supporting electrolyte leads to a merging of the redox waves accompanied by a shift to higher redox potentials. Prototype batteries manufactured with 10 wt % polymer as active material exhibit full material activity at the first charge/discharge cycle. During the first 100 cycles, the capacity drops to 50%. Higher contents of polymer (up to 40 wt %) leads to a lower material activity. Furthermore, the battery system reveals a fast charge/discharge ability, allowing a maximum speed up to 10C (6 min) with only a negligible loss of capacity.
ABSTRACT
The first polymer bearing exTTF units intended for the use in electrical charge storage is presented. The polymer undergoes a redox reaction involving two electrons at -0.20 V vs Fc/Fc(+) and is applied as active cathode material in a Li-organic battery. The received coin cells feature a theoretical capacity of 132 mAh g(-1) , a cell potential of 3.5 V, and a lifetime exceeding more than 250 cycles.
Subject(s)
Electric Power Supplies , Heterocyclic Compounds/chemistry , Lithium/chemistry , Polymers/chemistry , Electrodes , Free Radicals/chemistry , Ions/chemistry , Oxidation-Reduction , Polymers/chemical synthesisABSTRACT
Polymers with pendant phenoxyl radicals are synthesized and the electrochemical properties are investigated in detail. The monomers are polymerized using ring-opening metathesis polymerization (ROMP) or free-radical polymerization methods. The monomers and polymers, respectively, are oxidized to the radical either before or after the polymerization. These phenoxyl radicals containing polymers reveal a reversible redox behavior at a potential of -0.6 V (vs Ag/AgCl). Such materials can be used as anode-active material in organic radical batteries (ORBs).
Subject(s)
Electric Power Supplies , Phenols/chemistry , Polymers/chemistry , Free Radicals/chemistry , Oxidation-ReductionABSTRACT
An alkyne-functionalized ruthenium(II) bis-terpyridine complex is directly copolymerized with phenylacetylene by alkyne polymerization. The polymer is characterized by size-exclusion chromatography (SEC), (1) H NMR spectroscopy, cyclic voltammetry (CV) measurements, and thermal analysis. The photophysical properties of the polymer are studied by UV-vis absorption spectroscopy. In addition, spectro-electrochemical measurements are carried out. Time-resolved luminescence lifetime decay curves show an enhanced lifetime of the metal complex attached to the conjugated polymer backbone compared with the Ru(tpy)2 (2+) model complex.
