Hexafluorobenzene (C6F6) strongly solvated the porphyrin ring via a quadrupolar interaction. The solvation sphere of C6F6 hindered the thermal fluctuations near the porphyrin ring and evoked remarkable photoelectronic properties of the porphyrins such as fluorescence enhancement and spectral sharpening due to confined torsional planarity.

A comprehensive study of supramolecular polymerization of ditopic zinc (2-pyridylethynyl)porphyrin dimer 1 in toluene and thin films was performed. A glass-forming porphyrin bearing 3,4,5-tri((S)-3,7-dimethyloctyloxy)phenyl groups, named “porphyrin glass”, was introduced with the 2-pyridylethynyl group as a supramolecular organizing unit; two zinc (2-pyridylethynyl)porphyrins were held together by self-complementary pyridyl-to-zinc coordination bonds to form a slipped-cofacial stack. Then, ditopic zinc (2-pyridylethynyl)porphyrin could be extended to a linear supramolecular polymer. The small binding constant limited the degree of supramolecular polymerization of 1 in toluene solution. In spin-cast film, on the other hand, 1 adopted a form of supramolecular polymer of porphyrin glass, which was effective enough to display a large bathochromic shift of the absorption bands exceeding the narrowest limit of the optical band gap extrapolated from the electronic structures in solution. The supramolecularly polymerized porphyrin glass formed excimer, which exhibited solid-state near-infrared (NIR) luminescence at approximately 1025 nm.

A metal-lustrous self-standing film, named “porphyrin foil”, was formed from a glass-forming polymeric porphyrin. The amorphous glass nature of the porphyrin foil played a key role in spontaneously producing a smooth surface. Its sharp contrast in intense absorption and specular reflection of light at each wavelength provided a brilliant metallic lustre.

The amorphous nature of a series of zinc–porphyrins bearing two 3,4,5-tri((S)-3,7-dimethyloctyloxy)phenyl groups at the meso-positions, named “porphyrin glass”, were tolerant of π-conjugation engineering in ethynylene-linked dimers. The butadiyne-linked dimeric porphyrin glass formed an intermolecular excimer, which exhibited bright and exceptionally long-lived, near-infrared (NIR) luminescence at approximately 970 nm in the solid state. Therefore, porphyrin glasses overcame a general bottleneck for NIR-luminescence, such as an undesired π-stacked aggregation of a large porphyrin plane in addition to the energy gap law. The formation of amorphous molecular glasses from a series of meso-ethynylene-conjugated zinc–porphyrins, named “porphyrin glass”, is described. The butadiyne-linked dimeric porphyrin glass formed an intermolecular excimer, which exhibited solid-state, near-infrared (NIR) luminescence at approximately 970 nm.

An oligoamylose-strapped porphyrin displayed circularly polarized luminescence (CPL) in the S1 state despite being silent in circular dichroism (CD) in the ground state, suggesting chirality induction in the photoexcited porphyrin moiety from the oligoamylose-strap in the photoexcited state.

The considerably conjugated π systems of the group 14 dithienometallole-linked ethynylene-conjugated porphyrin dimers (1Ms) were described based on comprehensive experimental and theoretical studies. The electronic absorption spectra of 1M displayed a large splitting in the Soret band and a red-shifted Q-band, indicating that the dithienometallole spacer was effective in facilitating the porphyrin–porphyrin electronic coupling. Torsional planarization behaviors of 1M were observed in the time-resolved fluorescence spectra. Density functional theory (DFT) calculations revealed that the dithienometallole spacer is an ideal partner for the ethynylene-conjugated porphyrin to produce fully delocalized highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) levels due to their similar HOMO and LUMO levels. Finally, 1M exhibited a strong propensity for the quinoidal–cummulenic conjugation in the dithienometallole spacer when in a photoexcited state.

Oligomeric porphyrin arrays with an alternating pyridyl–porphyrin sequence were synthesized to explore double-strand formation through self-complementary pyridyl-to-zinc axial coordination bonds. Competitive titration experiments revealed the thermodynamic aspects involved in the zipper effect within double-strand formation. Multiple axial coordination bonds defined the stacked conformation, despite a marginal contribution to the stability of the double-strands. Thus, the zipper cooperativity was the dominant factor for the remarkable stability. Moreover, the dimeric and trimeric porphyrin arrays were independently assembled into double-strands by self-sorting from a binary mixture. Double-strand formation engineered discretely stacked π-systems. Successive slipped-cofacial stacks of the porphyrin rings progressively extended the π-system via exciton coupling over the double-strand while keeping a relatively high fluorescence quantum yield.

A novel binuclear phthalocyanine tweezers, in which two zinc-phthalocyanine rings are linked to an optically active binaphthyl group through triazolyl linkages, was self-cyclized through triazolyl-to-zinc coordination bonds. An axially chiral S-binaphthyl group induced planar chirality in a slipped-cofacial stack of phthalocyanine moieties, and therefore displayed fluorescence with a good quantum yield (ΦF = 0.23) and circularly polarized luminescence with a moderate intensity of dissymmetry factor (glum = −4 × 10−4) in the near-infrared wavelength region.

The synthesis of a dendron composed of tetrameric subphthalocyanine (SubPc) is accomplished by substituting the chlorine groups with phenoxy groups at the axial positions of SubPc with SubPc-triol. The present molecular design of the SubPc-triol introduces three phenol groups at the peripheral positions of the SubPc macrocycle as a tritopic template to construct SubPc dendrons. The self-polycondensation of SubPc-triol as a ‘divergent’ synthesis only gave a trace amount of the hyperbranched arrays due to poor solubility of the SubPc-triol. In contrast, a ‘convergent’ synthesis with the terminal SubPc improved the solubility throughout the reaction and a tetrameric SubPc dendron was obtained in moderate isolated yield.

Supramolecular control of the π-stacked configuration of aqueous phthalocyanine (Zn[Pc(SO3)4]) was achieved, allowing organization of a J-type slipped-cofacial dimer with per-O-methylated α-cyclodextrin (TMe-α-CDx) by the aid of host–guest interactions. Pristine Zn[Pc(SO3)4] forms nonfluorescent face-to-face aggregates in water. The π-stacked configuration was controlled in the slipped-cofacial dimer, which was formed as a shallow inclusion complex with TMe-α-CDx, giving remarkably enhanced fluorescence with a very small Stokes shift. Organization of the J-type slipped-cofacial dimer as a 2:2 Zn[Pc(SO3)4]–TMe-α-CDx complex was achieved through π-stacking of the unencapsulated segment of Zn[Pc(SO3)4] shallowly encapsulated by a small TMe-α-CDx cavity.

A highly congested hexameric subphthalocyanine array was synthesized by axial chlorine-to-phenoxy substitution of a hexakis(4-hydroxyphenyl)benzene based subphthalocyanine, and photoinduced symmetry-breaking charge separation was demonstrated in polar solvent.

Bolaamphiphilic zinc porphyrins bearing a 2-pyridylethynyl or 4-methoxyphenylethynyl group, Zn(PyPor) or Zn(ArPor), respectively, were newly synthesized in order to explore the molecular organizing behaviours within the interior hydrophobic layer of aqueous self-assemblies. Well-ordered J-type aggregates of Zn(PyPor) were formed in aqueous self-assembled bolaamphiphile, whereas J-type aggregates of Zn(ArPor) were disordered. The titration experiments suggest that axial coordination bond improves the structural uniformity of the J-type aggregates of Zn(PyPor). In a homogeneous isotropic media, on the other hand, Zn(PyPor) formed an antiparallel dimer through self-complementary coordination. Unprecedented molecular organization of ligand-assisted J-type aggregates is described in the term of anticooperative effect under the bulk conditions.

Oligomeric porphyrin arrays with an alternating pyridyl–porphyrin sequence were synthesized to explore double-strand formation through self-complementary pyridyl-to-zinc axial coordination bonds. Competitive titration experiments revealed the thermodynamic aspects involved in the zipper effect within double-strand formation. Multiple axial coordination bonds defined the stacked conformation, despite a marginal contribution to the stability of the double-strands. Thus, the zipper cooperativity was the dominant factor for the remarkable stability. Moreover, the dimeric and trimeric porphyrin arrays were independently assembled into double-strands by self-sorting from a binary mixture. Double-strand formation engineered discretely stacked π-systems. Successive slipped-cofacial stacks of the porphyrin rings progressively extended the π-system via exciton coupling over the double-strand while keeping a relatively high fluorescence quantum yield.

An oligoamylose-strapped porphyrin displayed circularly polarized luminescence (CPL) in the S1 state despite being silent in circular dichroism (CD) in the ground state, suggesting chirality induction in the photoexcited porphyrin moiety from the oligoamylose-strap in the photoexcited state.

Bolaamphiphilic zinc porphyrins bearing a 2-pyridylethynyl or 4-methoxyphenylethynyl group, Zn(PyPor) or Zn(ArPor), respectively, were newly synthesized in order to explore the molecular organizing behaviours within the interior hydrophobic layer of aqueous self-assemblies. Well-ordered J-type aggregates of Zn(PyPor) were formed in aqueous self-assembled bolaamphiphile, whereas J-type aggregates of Zn(ArPor) were disordered. The titration experiments suggest that axial coordination bond improves the structural uniformity of the J-type aggregates of Zn(PyPor). In a homogeneous isotropic media, on the other hand, Zn(PyPor) formed an antiparallel dimer through self-complementary coordination. Unprecedented molecular organization of ligand-assisted J-type aggregates is described in the term of anticooperative effect under the bulk conditions.

A highly congested hexameric subphthalocyanine array was synthesized by axial chlorine-to-phenoxy substitution of a hexakis(4-hydroxyphenyl)benzene based subphthalocyanine, and photoinduced symmetry-breaking charge separation was demonstrated in polar solvent.