Akiharu Satake

Artificial photosynthetic systems: assemblies of slipped cofacial porphyrins and phthalocyanines showing strong electronic coupling

This paper reviews selected types of structurally well defined assemblies of porphyrins and phthalocyanines with strong electronic coupling. Face-to-face, head-to-tail, slipped cofacial, and non-parallel dimeric motifs constructed by covalent and non-covalent bonds are compared in the earlier sections. Their molecular orientation, electronic overlap, and absorption and fluorescence properties are discussed with a view towards the development of artificial photosynthetic systems and molecular electronics. Complementary coordination dimers are fully satisfactory in terms of structural stability, orientation factor, pi-electronic overlap, and zero fluorescence quenching. In later sections, several polymeric and macrocyclic porphyrin assemblies constructed by a combination of covalent bonds and complementary coordination bonds are discussed from the viewpoint of light-harvesting antenna functions.

An Artificial Ion Channel Formed by a Macrocyclic Resorcin[4]arene with Amphiphilic Cholic Acid Ether Groups

Tail-to-tail assembly of two molecules of a resorcin[4]arene resulted in a bilayer membrane with an intramembrane ion channel. The steroidal tails introduced here have the advantages of giving a long-lived open state of the pore (2.5-4.5 s, as opposed to tens of milliseconds for alkyl tails) and of allowing the hydrophilic pore to be modified without changing the overall structural features.

Transmembrane nanopores from porphyrin supramolecules.

A porphyrin-based nanopore was constructed through a bilayer lipid membrane (BLM). The macrocyclic porphyrin (the inner diameter = ca. 2.1 nm) having six carboxylic acid groups directed up and down was synthesized by self-assembly of three trisporphyrins, metathesis linking, and subsequent hydrolysis. The porphyrin was incorporated into soybean lecithin based BLM, and the ion currents through the nanopore were observed under 500 mM KCl, LiCl, CaCl2, and tetraalkylammonium chloride solutions, indicating formation of a large pore through BLM. Blocking of the ion current was achieved by addition of the polycationic fourth-generation PAMAM dendrimer.

Energy Transfer Followed by Electron Transfer in a Porphyrin Macrocycle and Central Acceptor Ligand: A Model for a Photosynthetic Composite of the Light‐Harvesting Complex and Reaction Center

A system that models a photosynthetic composite of the light-harvesting complex and reaction center is reported in which light energy collected by cyclic antenna porphyrins is transferred to a central energy-acceptor porphyrin, followed by photoinduced electron transfer to a fullerene positioned above the ring plane. Pyridyl tripodal ligands appended with bis(phenylethynyl)porphyrinatozinc(II) (ZnP-Tripod) and additional fulleropyrrolidine moieties (C(60)-ZnP-Tripod) were synthesized as the reaction center units. The tripodal ligand was strongly accommodated by the light-harvesting porphyrin macrocycle N-(1-Zn)(3) (1-Zn = trisporphyrinatozinc(II)) by using three-point coordination of pyridyl to uncoordinated porphyrinatozinc sites to afford a stable 1:1 composite. The binding constants for ZnP-Tripod and C(60)-ZnP-Tripod in benzonitrile were estimated from steady-state fluorescence titrations to be 1.4x10(7) and 1.6x10(7) M(-1), respectively. The steady-state fluorescence titration, fluorescence lifetime, and transient absorption studies revealed that in both composites the excitation energy collected by the nine porphyrins of N-(1-Zn)(3) was efficiently transferred to a ZnP moiety by means of a through-space mechanism with a quantum yield of approximately 90%. Furthermore, in the composite with C(60)-ZnP-Tripod, the converged energy at the ZnP moiety induced electron transfer to the C(60) moiety, which afforded the stable charge-separated state (Phi(CS)>90%).

Light-Harvesting Supramolecular Porphyrin Macrocycle Accommodating a Fullerene–Tripodal Ligand

Trisporphyrinatozinc(II) (1-Zn) with imidazolyl groups at both ends of the porphyrin self-assembles exclusively into a light-harvesting cyclic trimer (N-(1-Zn)(3)) through complementary coordination of imidazolyl to zinc(II). Because only the two terminal porphyrins in 1-Zn are employed in ring formation, macrocycle N-(1-Zn)(3) leaves three uncoordinated porphyrinatozinc(II) groups as a scaffold that can accommodate ligands into the central pore. A pyridyl tripodal ligand with an appended fullerene connected through an amide linkage (C(60)-Tripod) was synthesized by coupling tripodal ligand 3 with pyrrolidine-modified fullerene, and this ligand was incorporated into N-(1-Zn)(3). The binding constant for C(60)-Tripod in benzonitrile reached the order of 10(8) M(-1). This value is ten times larger than those of pyridyl tetrapodal ligand 2 and tripodal ligand 3. This behavior suggests that the fullerene moiety contributes to enhance the binding of C(60)-Tripod in N-(1-Zn)(3). The fluorescence of N-(1-Zn)(3) was almost completely quenched (approximately 97 %) by complexation with C(60)-Tripod, without any indication of the formation of charge-separated species or a triplet excited state of either porphyrin or fullerene in the transient absorption spectra. These observations are explained by the idea that the fullerene moiety of C(60)-Tripod is in direct contact with the porphyrin planes of N-(1-Zn)(3) through fullerene-porphyrin pi-pi interactions. Thus, C(60)-Tripod is accommodated in N-(1-Zn)(3) with a pi-pi interaction and two pyridyl coordinations. The cooperative interaction achieves a sufficiently high affinity for quantitative and specific introduction of one equivalent of tripodal guest into the antenna ring, even under dilute conditions ( approximately 10(-7) M) in polar solvents such as benzonitrile. Additionally, complete fluorescence quenching of N-(1-Zn)(3) when accommodating C(60)-Tripod demonstrates that all of the excitation energy collected by the nine porphyrins migrates rapidly over the macrocycle and then converges efficiently on the fullerene moiety by electron transfer.

Synthesis and structural analysis of palladium(II) pyridinylpyrazole complexes by 1H-, 13C-, 15N-NMR and X-ray diffraction. Comparison of binuclear methylpalladium, chloromethylpalladium, and dichloropalladium complexes by 15N-NMR

Abstract MePdCl[3-methyl-5-(2-pyridinyl)pyrazole] (1 and 2), PdCl2[3-methyl-5-(2-pyridinyl)pyrazole] (3), and bis{MePd[3-methyl-5-(2-pyridinyl)pyrazole]} (4) were synthesized, and structural assignment was performed by 1H-, 13C-, 15N-NMR spectroscopy. By comparison of their 15N-NMR spectra, the relationship between bond strength of the palladiumnitrogen bond and chemical shift was analyzed. X-ray diffraction analysis of 4 was also achieved.

Asymmetric cyclopropanation of ketene silyl acetal with allylic acetate catalyzed by a palladium complex

Abstract The first asymmetric cyclopropanation of ketene silyl acetal with allylic acetate was achieved. New chiral oxazolidinylpyrazole ligands and their η 3 -allylpalladium complexes were synthesized. Reaction of cinnamyl acetate with ketene silyl acetal of ethyl isobutylate in the presence of a palladium complex gave a phenyl cyclopropane derivative in 20∼ 54%ee.

Supramolecular Organization of Light-Harvesting Porphyrin Macrorings

Porphyrin-based supramolecular nanostructures have been produced by the self-assembly of porphyrin macrorings with three benzoic acid groups (Acid-R) on each side of the rings through cooperative carboxyl-carboxyl hydrogen bonds. Structures of the organized Acid-R were analyzed by AFM, and two clear distribution peaks were observed at 3 and 27 nm in the height-distribution histogram. From the overall assessment, the higher objects are considered to be one-dimensional structures standing vertically on the mica substrate. The height corresponds to an 11-mer of a unit Acid-R. Light-harvesting functions were examined by using fluorescence titration, whereby an energy-acceptor molecule (Tripod 2) was employed that strongly interacted with Acid-R units (association constant: 2.0×10(8)  M(-1) ), specifically from the inner pore. The titration results showed that the apparent stoichiometry [Tripod 2]/[Acid-R] was <0.5, and that the value was concentration dependent. Titration results reasonably account for the scheme in which Tripod 2 only interacts with each terminal in the organized Acid-R. The number of organization was fitted to a 10-mer of Acid-R in a 6.8×10(-7)  M solution, and was consistent with that estimated from the AFM results. In the composites of organized Acid-R/Tripod 2, a singlet excitation energy transfer occurred among the Acid-R units, and to Tripod 2. The energy-transfer rate constants were estimated by using the decamer model, which employed kinetic parameters obtained from steady-state and time-resolved fluorescence experiments.

Tetracyanoresorcin[4]arene as a pH dependent artificial acetylcholine receptor

This communication describes the facile synthesis of tetracyanoresorcin[4]arene and its high and pH dependent affinities toward biologically important acetylcholine in the physiological pH region.

Construction of giant porphyrin macrorings self-assembled from thiophenylene-linked bisporphyrins for light-harvesting antennae.

As a model of bacterial photosynthetic light-harvesting antenna, a large number of porphyrin units were organized into barrel-shaped macrorings. Two imidazolylporphyrinatozinc(II) molecules were linked through either unsubstituted thiophenes or 3,4-dioctylthiophenes 1 a and 1 b, respectively. These structures were spontaneously organized by complementary coordination of the imidazolyl to zinc and produced a series of self-assembled fluorescent polygonal macrorings under high dilution conditions. The ring size increased compared with previous m-phenylene examples. The size distribution was also controlled by the presence of octyl substituents. A wide distribution of macrorings from 7- to >15-mer was obtained from 1 a, whereas macrorings ranging from 7- to 11-mer with a maximum population focused at the 8-mer were formed with 1 b. The size distribution was governed by competition between entropy-favored, smaller-ring formation and the enthalpy-favored, less-strained larger macroring. The UV/Vis spectra showed a gradual redshift for the larger rings reflecting an increase in the transition dipole interactions.