A new approach for the photosynthetic antenna-reaction center complex with a model organized around an s-triazine linker.

Two new artificial mimics of the photosynthetic antenna-reaction center complex have been designed and synthesized (BDP-H2 P-C60 and BDP-ZnP-C60). The resulting electron-donor/acceptor conjugates contain a porphyrin (either in its free-base form (H2P) or as Zn-metalated complex (ZnP)), a boron dipyrrin (BDP), and a fulleropyrrolidine possessing, as substituent of the pyrrolidine nitrogen, an ethylene glycol chain terminating in an amino group C60-X-NH2 (X=spacer). In both cases, the three different components were connected by s-triazine through stepwise substitution reactions of cyanuric chloride. In addition to the facile synthesis, the star-type arrangement of the three photo- and redox-active components around the central s-triazine unit permits direct interaction between one another, in contrast to reported examples in which the three components are arranged in a linear fashion. The energy- and electron-transfer properties of the resulting electron-donor/acceptor conjugates were investigated by using UV/Vis absorption and emission spectroscopy, cyclic voltammetry, and femtosecond transient absorption spectroscopy. Comparison of the absorption spectra and cyclic voltammograms of BDP-H2P-C60 and BDP-ZnP-C60 with those of BDP-H2P, BDP-ZnP and BDP-C60, which were used as references, showed that the spectroscopic and electrochemical properties of the individual constituents are basically retained, although some appreciable shifts in terms of absorption indicate some interactions in the ground state. Fluorescence lifetime measurements and transient absorption experiments helped to elucidate the antenna function of BDP, which upon selective excitation undergoes a rapid and efficient energy transfer from BDP to H2P or ZnP. This is then followed by an electron transfer to C60, yielding the formation of the singlet charge-separated states, namely BDP-H2(·+) -C60(·-) and BDP-ZnP(·+)-C60(·-). As such, the sequence of energy transfer and electron transfer in the present models mimics the events of natural photosynthesis.

Fullerene-coumarin dyad as a selective metal receptor: synthesis, photophysical properties, electrochemistry and ion binding studies.

A coumarin derivative with a malonate unit has been synthesized and used for the preparation of a fullerene-coumarin dyad through the Bingel cyclopropanation method. The newly synthesized dyad is soluble in organic solvents and has been fully characterized with traditional spectroscopic techniques. Electronic interactions between the two components of the dyad were probed with the aid of UV/Vis spectroscopy, fluorescence emission, and electrochemistry measurements. Our studies clearly show the presence of electronic interactions between C(60) and modified coumarin in the ground state; efficient electron-transfer quenching of the singlet excited state of the coumarin moiety by the appended fullerene sphere was also observed. Time-resolved fluorescence measurements revealed lifetimes for the coumarin-C(60) dyad at a maximum of 50 ps, while the quantum yield was reaching unity. Additionally, the redox potentials of the C(60)-coumarin dyad were determined and the energetics of the electron-transfer processes were evaluated. Finally, after alkaline treatment of C(60)-coumarin, which resulted in the deprotection of carboxylate units, the dyad was tested as a metal receptor for divalent metal cations; ion competition studies and fluorescence experiments showed binding selectivity for lead ions.

Azafullerenes encapsulated within single-walled carbon nanotubes.

Methods of insertion of azafullerenes in single-walled carbon nanotubes (SWNTs) at different temperatures were investigated, while the effects of the conditions applied on the structure of azafullerene-based peapods, namely, C59N@SWNTs, were explored. Morphological characteristics of C59N@SWNTs were assessed and evaluated by means of high-resolution transmission electron microscopy (HR-TEM). Pathways and chemical reactions that occur upon encapsulation of C59N within SWNTs were evaluated. Monomeric azafullerenyl radical C59N. as inserted into SWNTs at high temperature, from purified (C59N)2 in the gas phase, can undergo a variety of different transformations forming dimers, oligomers or existing in its monomeric form inside SWNTs due to the stabilization effect by nanotube side walls. However, under milder conditions, that is, at lower temperature, bisazafullerene (C59N)2 can be inserted into SWNTs in its pristine dimeric form.

Stability, thermal homolysis and intermediate phases of solid hydroazafullerene C59HN.

Density functional (DFT) calculations, high-temperature electron paramagnetic resonance (EPR) and transmission electron microscopy (TEM) results suggest that thermal homolysis of C59HN involves a remarkably stable intermediate C59N-C59HN* structure characterised by charge redistribution from a C59N* radical to a bonded C59HN.

Soluble functionalized carbon nanohorns.

Carbon nanahorns (CNH) were functionalized following the methodology of 1,3-dipolar cycloaddition of azomethine ylides and found to form stable solutions in either organic solvents or water. The number of added functional units, in the form of pyrrolidine moieties, was calculated when a pyrene chromophore was utilized in the modification scheme. Moreover, complementary theoretical calculations revealed that reactivity enhancement is expected at locations near the conical-shaped tip of CNH, where the highest curvature and strain exist. Finally, additional organic transformation of already modified CNH was exploited by covalently linked ferrocene units.

Carbon nanotubes: materials for medicinal chemistry and biotechnological applications.

Carbon nanotubes are considered as molecular wires exhibiting novel properties for diverse applications including medicinal and biotechnological purposes. Surface chemistry on carbon nanotubes results on their solubilization in organic solvents and/or aqueous/physiological media. Herein, we will present how interfacing such novel carbon-based nanomaterials with biological systems may lead to new applications in diagnostics, vaccine and drug delivery. Recent developments in this rapidly growing field will be presented thus suggesting exciting opportunities for the utilization of carbon nanotubes as useful tools for biotechnological applications. Emphasis will be placed in the integration of biomaterials with carbon nanotubes, which enables the use of such hybrid systems as biosensor devices, immunosensors and DNA-sensors.

Electronic interplay on illuminated aqueous carbon nanohorn-porphyrin ensembles.

Tetracationic water-soluble porphyrin (H(2)P(4+)) has been immobilized by pi-pi stacking interactions onto the skeleton of carbon nanohorns (CNH), without disrupting their pi-electronic network. The stable aqueous solution of the CNH-H(2)P(4+) nanoensemble was examined by both electron microscopy and spectroscopic techniques. The efficient fluorescence quenching of the H(2)P(4+) moiety in the CNH-H(2)P(4+) nanoensemble was probed by steady-state as well as time-resolved fluorescence emission spectroscopy, suggesting charge separation from the photoexcited H(2)P(4+) to CNH. In the presence of methyl viologen dication (MV(2+)) and a hole trap, accumulation of the reduced species of methyl viologen was observed by the photoillumination of CNH-H(2)P(4+), suggesting that the electron migration from the initially formed charge-separated state takes place. Transient absorption spectroscopy gave further insights on the transient species such as the charge-separated state (CNH(*-))-(H(2)P(4+))(*+), which was consumed in the presence of MV(2+) and hole shifter, leaving the reduced methyl viologen.

Exfoliated semiconducting pure 2H-MoS2 and 2H-WS2 assisted by chlorosulfonic acid.

Chlorosulfonic acid assisted the exfoliation of MoS2 and WS2 resulting in retaining their semiconducting 2H-phase, sharply contrasting the semiconducting-to-metallic phase-transition observed with the currently available exfoliation techniques.

Reductive dismantling and functionalization of carbon nanohorns.

Reduction of carbon nanohorn (CNH) aggregates with potassium naphthalenide resulted in their dismantling and individualization. Furthermore, the reduced CNHs were functionalized via addition of electrophiles.

Donor-acceptor graphene-based hybrid materials facilitating photo-induced electron-transfer reactions.

Graphene research and in particular the topic of chemical functionalization of graphene has exploded in the last decade. The main aim is to increase the solubility and thereby enhance the processability of the material, which is otherwise insoluble and inapplicable for technological applications when stacked in the form of graphite. To this end, initially, graphite was oxidized under harsh conditions to yield exfoliated graphene oxide sheets that are soluble in aqueous media and amenable to chemical modifications due to the presence of carboxylic acid groups at the edges of the lattice. However, it was obvious that the high-defect framework of graphene oxide cannot be readily utilized in applications that are governed by charge-transfer processes, for example, in solar cells. Alternatively, exfoliated graphene has been applied toward the realization of some donor-acceptor hybrid materials with photo- and/or electro-active components. The main body of research regarding obtaining donor-acceptor hybrid materials based on graphene to facilitate charge-transfer phenomena, which is reviewed here, concerns the incorporation of porphyrins and phthalocyanines onto graphene sheets. Through illustrative schemes, the preparation and most importantly the photophysical properties of such graphene-based ensembles will be described. Important parameters, such as the generation of the charge-separated state upon photoexcitation of the organic electron donor, the lifetimes of the charge-separation and charge-recombination as well as the incident-photon-to-current efficiency value for some donor-acceptor graphene-based hybrids, will be discussed.

Photoinduced electron transfer on aqueous carbon nanohorn-pyrene-tetrathiafulvalene architectures.

Water-soluble carbon-nanohorn-tetrathiafulvalene (CNH-TTF) nanoensembles were prepared by utilizing positively charged pyrene as an assembly medium and characterized by spectroscopy and electron microscopy. Electronic interactions within the nanoensemble were probed by optical spectroscopy, indicating electron transfer between the TTF units and CNHs after light illumination.

Composition and insect attracting activity of the essential oil of Rosmarinus officinalis.

The essential oil and a number of extracts of Rosmarinus officinalis L. in solvents of increasing polarity were isolated, and their components identified and tested as pest control agents. Ethanol and acetone extracts attract grape berry moth Lobesia botrana. However, none of the extracts had a significant effect on western flower thrips Frankliniella occidentalis, which is attracted by 1,8-cineole, a major essential oil component.

Correction of the structure of a new sesquiterpene from Cistus creticus ssp. creticus.

In an attempt to identify the structure of a sesquiterpene from Cistus creticus ssp. creticus proposed in the literature as 1,1,4a,6-tetramethyl-5-methylene-1,2,3,4,4alpha,5,8,8alpha-octahydronaphthalene, the synthesis of its cis isomer 2 was carried out in 11 steps and 9.5% yield. Comparison of the spectra of 2 and those reported earlier for the synthetic trans isomer 1 with the spectral profile of the isolated natural product indicated that the latter was not compatible with either 1 or 2. The correct structure was assigned, by detailed spectroscopic analysis of the natural product, as 6-isopropenyl-4,4a-dimethyl-1,2,3,4,4a,5,6,7-octahydronaphthalene (3).