Michaela Ruppert

Tetrathiafulvalene-Based Nanotweezers—Noncovalent Binding of Carbon Nanotubes in Aqueous Media with Charge Transfer Implications

Electron donor-acceptor hybrids based on single wall carbon nanotubes (SWCNT) are one of the most promising functional structures that are currently developed in the emerging areas of energy conversion schemes and molecular electronics. As a suitable electron donor, π-extended tetrathiafulvalene (exTTF) stands out owing to its recognition of SWCNT through π-π stacking and electron donor-acceptor interactions. Herein, we explore the shape and electronic complementarity between different types of carbon nanotubes (CNT) and a tweezers-shaped molecule endowed with two exTTFs in water. The efficient electronic communication between semiconducting SWCNT/multiwall carbon nanotubes (MWCNT), on one hand, and the water-soluble exTTF nanotweezers 8, on the other hand, has been demonstrated in the ground and excited state by using steady-state as well as time-resolved spectroscopies, which were further complemented by microscopy. Importantly, appreciable electronic communication results in the electronic ground state having a shift of electron density, that is, from exTTFs to CNT, and in the electronic excited state having a full separation of electron density, that is oxidized exTTF and reduced CNT. Lifetimes in the range of several hundred picoseconds, which were observed for the corresponding electron transfer products upon light irradiation, tend to be appreciably longer in MWCNT/8 than in SWCNT/8.

Mutual interplay of light harvesting and triplet sensitizing in a perylene bisimide antenna-fullerene dyad.

A flexible organic dyad consisting of a perylene bisimide antenna covalently linked to a [60]fullerene has been synthesized and studied by electrochemistry, steady-state spectroscopy, and time-resolved spectroscopy. We found that the energy absorbed by the perylene bisimide is transferred to the fullerene with an efficiency close to 100%. The fullerene in turn undergoes intersystem crossing followed by triplet energy transfer back to the perylene bisimide with an efficiency of at least 20%. Hence the perylene bisimide unit acts as an antenna for the fullerene, i.e., effectively extending the fullerene absorption far into the visible spectral range, while at the same time the fullerene acts as a triplet sensitizer for the perylene bisimide. This has severe consequences for the exploitation of the dye antenna-fullerene concept for light harvesting in solar cells.

trans-2 Addition Pattern to Power Charge Transfer in Dendronized Metalloporphyrin C60 Conjugates

Coordinating different transition metals--manganese(III), iron(III), nickel(II), and copper(II)--by a dendronized porphyrin afforded a new family of redox-active metalloporphyrins to which C(60) was attached as a ground-state electron acceptor. Such a strategy introduced an additional center of redoxactivity, that is, a change of the oxidation state of the metal. Cyclic voltammetry and absorption/fluorescence measurements provided support for mutual interactions between the redox-active constituents in the ground state. In particular, slightly anodic shifted reduction potentials/cathodic shifted oxidation potentials and the occurrence of new charge transfer features in the 700-900 nm range prompt to sizable electronic coupling in the range of 300 cm(-1). Photophysical means--steady-state/time-resolved fluorescence and transient absorption measurements--shed light on the excited-state interactions. To this end, we have added pulse radiolytic investigations to characterize the radical cation (i.e., metalloporphyrins) and radical anion (i.e., fullerene) characteristics. Pi-pi stacking of the excited state electron donor and the electron acceptor is key to overcome the intrinsically fast deactivation of the excited states in these metalloporphyrins and to power an exothermic charge transfer. The lifetimes of the rapidly and efficiently generated radical ion pair states, which range from 15 to >3000 ps, revealed several important trends. First, they were found to depend on the solvent polarity. Second, the nature of the transition metal plays a similarly decisive role. It is important that the product of charge recombination, namely tripmultiplet excited states versus ground state, had a great impact. Finally, a correlation between the charge transfer rate (i.e., charge separation and charge recombination) and the free energy change for the underlying reaction reveals a parabolic dependence with parameters of the reorganization energy (0.84 eV) and electronic coupling (70 cm(-1)) closely resembling that seen for the zinc(II) and free base analogues.

A charge-transfer challenge: combining fullerenes and metalloporphyrins in aqueous environments.

A series of truly water-soluble C(60)/porphyrin electron donor-acceptor conjugates has been synthesized to serve as powerful mimics of photosynthetic reaction centers. To this end, the overall water-solubility of the conjugates was achieved by adding hydrophilic dendrimers of different generations to the porphyrin moiety. An important variable is the metal center of the porphyrin; we examined zinc(II), copper(II), cobalt(II), nickel(II), iron(III), and manganese(III). The first insights into electronic communication between the electron donors and the electron acceptors came from electrochemical assays, which clearly indicate that the redox processes centered either on C(60) or the porphyrins are mutually affected. Absorption measurements, however, revealed that the electronic communication in terms of, for example, charge-transfer features, remains spectroscopically invisible. The polar environment that water provides is likely to be a cause of the lack of detection. Despite this, transient absorption measurements confirm that intramolecular charge separation processes in the excited state lead to rapid deactivation of the excited states and, in turn, afford the formation of radical ion pair states in all of the investigated cases. Most importantly, the lifetimes of the radical ion pairs were found to depend strongly on several aspects. The nature of the coordinated metal center and the type of dendrimer have a profound impact on the lifetime. It has been revealed that the nature/electronic configuration of the metal centers is decisive in powering a charge recombination that either reinstates the ground state or any given multiplet excited state. Conversely, the equilibrium of two opposing forces in the dendrimers, that is, the interactions between their hydrophilic regions and the solvent and the electronic communication between their hydrophobic regions and the porphyrin and/or fullerene, is the key to tuning the lifetimes.

Dendronizing and Metalating trans‐2 C60 Tetraaryl Porphyrins—A Versatile Approach Toward Water‐Soluble Donor–Acceptor Conjugates

We have realized for the first time a series of truly water-soluble and tightly coupled porphyrin/C(60) electron-donor-acceptor conjugates in which the charge separation and charge recombination dynamics are controlled by modifying the nature of the dendrimer and/or the choice of the central metal atom.

Dendronized Fullerene–Porphyrin Conjugates in ortho, meta, and para Positions: A Charge-Transfer Assay

The physicochemical characterization, that is, ground and excited state, of a new series of dendronized porphyrin/fullerene electron donor-acceptor conjugates in nonaqueous and aqueous environments is reported. In contrast to previous work, we detail the charge-separation and charge-recombination dynamics in zinc and copper metalloporphyrins as a function of first- and second-generation dendrons as well as a function of ortho, meta, and para substitution. Both have an appreciable impact on the microenvironments of the redox-active constituents, namely the porphyrins and the fullerenes. As a matter of fact, the resulting charge-transfer dynamics were considerably impacted by the interplay between the associated forces that reach from dendron-induced shielding to dipole-charge interactions.

Dendritic Metalloporphyrin–Fullerene Conjugates: Changing the Microenvironment around Redox‐Active Centers and its Impact on Charge‐Transfer Reactions

Photophysical investigations on a series of (2,4,6)-tris-substituted metalloporphyrin-fullerene conjugates revealed the effects of an electron-rich microenvironment surrounding the electron-donating porphyrin as a function of the metal center. On one hand, for all conjugates-water-soluble and non-water-soluble-ultrafast charge separation was observed upon photoexcitation. On the other hand, when examining the charge recombination dynamics for the non-water-soluble conjugates it becomes obvious that the (2,4,6)-tris-substitution stabilizes the radical-ion-pair state relative to the mono-substitution in the ortho-, meta-, and para-position. The more efficient protection of the electron-donating porphyrin from solvation is thought to be the major cause for this impact. Nevertheless, the situation is slightly different for the water-soluble conjugates. At first glance, the radical-ion-pair state lifetimes are, also in the case of the (2,4,6)-tris-substitution, longer than for the mono-substituted ortho-, meta- and para-conjugates. Upon closer inspection, they fail, however, to exhibit any metal dependence. Competing with the protection from solvation of the dendrons, dipole-charge interactions impact the stabilization in the polar aqueous environment and, in turn, become the dominant force governing the electron-transfer dynamics.

Microenvironment Engineering in ortho‐ and para‐Dendronized Metalloporphyrin–Fullerene Conjugates Involving a trans‐2‐Bisaddition Pattern

A new series of dendronized metalloporphyrin-fullerene conjugates as photosynthetic reaction center mimics was developed in a highly regioselective fashion through tether-controlled synthesis. The microenvironment around the porphyrin core is dependent on the spatial substitution pattern and the nature and generation number of the dendrons, which was proven by cyclic voltammetry.

Tailored heat treated accumulative roll bonded aluminum blanks: failure under bending stresses

Ultrafine-grained accumulative roll bonded (ARB) sheet metals of aluminum alloys have a high potential for lightweight construction. The mechanical properties can be enhanced regarding strength and ductility by the combination of ARB and a local heat treatment according to the Tailor Heat Treated Blanks technology. The present investigation focuses on the failure behavior of ultrafine-grained ARB blanks. Due to the low formability of these high-strength ARB metals, a detailed understanding of the failure mechanisms is essential. For this purpose, an established approach to determine the different stages of damage of the material for conventional materials is now applied to multilayered aluminum in the as-received and heat-treated condition. In this context, air bending tests are used to qualify and quantify the bending and forming behavior of ARB sheets of AA1050A and AA6016 aluminum alloys.