Synthesis of directly fused porphyrin dimers through Fe(OTf)3-mediated oxidative coupling.

An efficient and general Fe(OTf)3-mediated oxidative coupling method was developed for the synthesis of doubly or triply linked porphyrin dimers. Besides the central metal and peripheral substituent, regioselectivity of the oxidative coupling was found to be closely relevant to the onset oxidation potential of the porphyrin substrate, and the reactant with higher E(onset(ox)) tends to generate meso-ß doubly fused porphyrin dimer.

Clawlike tripodal porphyrin trimer: ion-controlled on­off fullerene binding.

A practical method for the preparation of novel tripodal tris(porphyrinato-urea) TP3 1 was readily achieved. Because of its appreciable preorganized triangular cone-shaped cavity resulting from the intramolecular hydrogen bonds of the tripodal tris-urea backbone, this porphyrin trimer host was found to have a high affinity toward fullerenes to form stable inclusion complexes in solution. A 120-fold binding selectivity toward C70 (Kassoc = 1.81 × 10(7) M(­1)) over C60 (Kassoc = 1.51 × 10(5) M(­1)) was further achieved in toluene. Moreover, the dissociation of such inclusion complexes can be easily realized by introducing H2PO4(­), and recapturing of the fullerene can be achieved after withdrawing H2PO4(­) by Ca(2+). A recyclable process for the inclusion and release of fullerene was therefore built by alternately feeding H2PO4(­) and Ca(2+). Benefiting from this approach, TP3 1 was sequentially applied to isolate C70 from the C60-enriched fullerene mixture successfully.

Metal-free iodine(III)-promoted synthesis of isoquinolones.

A metal-free oxidative cycloaddition reaction of substituted benzamides and alkynes has been developed for the synthesis of isoquinolones by using bis(trifluoracetoxy)iodobenzene (PIFA) and trifluoroacetic acid (TFA). Under mild conditions, a wide variety of isoquinolones were conveniently prepared via oxidative annulation of simple N-methoxybenzamide and diarylacetylene or aryl/alkyl acetylene derivatives in yields up to 87%.

Switchable regioselectivity in the PIFA-BF3·Et2O mediated oxidative coupling of meso-brominated Ni(II) porphyrin.

A simple and efficient method has been developed for the switchable synthesis of directly linked meso-brominated Ni(II) porphyrin dimers through PIFA-BF3·Et2O mediated oxidative coupling. The respective syntheses of meso-meso or meso-ß singly, doubly, and triply linked porphyrin dimers can be easily realized with the same reagent system.

High-speed microwave photonic switch for millimeter-wave ultra-wideband signal generation.

We propose a scheme for generating millimeter-wave (MMW) ultra-wideband (UWB) signal that is free from low-frequency components and a residual local oscillator. The system consists of two cascaded polarization modulators and is equivalent to a high-speed microwave photonic switch, which truncates a sinusoidal MMW into short pulses. The polarity switchability of the generated MMW-UWB pulse is also demonstrated.

Widely tunable single-bandpass microwave photonic filter based on polarization processing of a nonsliced broadband optical source.

We propose a new scheme of microwave photonic filter (MPF) based on the polarization processing of a broadband optical source (BOS), which features single-bandpass response and a wide span of operation bandwidth. The BOS is orthogonally polarized by a polarization division multiplexing emulator (PDME) with a tunable time delay between the two polarization states and incident at ± 45° to one principle axis of a polarization modulator (PolM). The PDME cascades a PolM, and a polarizer realizes a microwave modulation making the phase of the carrier able to be tuned while ± 1st sidebands remain unchanged, which after propagating in a dispersive medium results in a tunable single-bandpass response in the RF domain. We experimentally verify the MPF. By adjusting the time delay and the optical spectrum bandwidth, the passband center frequency is continuously tuned from DC to 20 GHz and the 3 dB passband bandwidth changes while the optical spectrum bandwidth ranges from 1 to 4 nm.

Chaotic ultra-wideband radio generator based on an optoelectronic oscillator with a built-in microwave photonic filter.

We induce a microwave photonic bandpass filter into an optoelectronic oscillator to generate a chaotic ultra-wideband signal in both the optical and electrical domain. The theoretical analysis and numerical simulation indicate that this system is capable of generating band-limited high-dimensional chaos. Experimental results coincide well with the theoretical prediction and show that the power spectrum of the generated chaotic signal basically meets the Federal Communications Commission indoor mask. The generated chaotic carrier is further intensity modulated by a 10 MHz square wave, and the waveform of the output ultra-wideband signal is measured for demonstrating the chaotic on-off keying modulation.

Photonic ultrawideband signal generator using an optically injected chaotic semiconductor laser.

We propose and demonstrate a method to generate ultrawideband (UWB) signals in the optical domain based on the chaotic dynamics of an optically injected semiconductor laser with optical feedback. The chaotic-UWB pulses with a fractional bandwidth of 116% and central frequency of 6.88 GHz are experimentally generated by controlling the injection strength and frequency detuning of the chaotic laser. The spectrum of the UWB signals is in full compliance with the Federal Communications Commission spectral mask, and the experimental results are qualitatively consistent with the simulated results.

Photonic generation of ultrawideband pulse using semiconductor laser with optical feedback.

We propose and demonstrate an approach to the generation of an ultrawideband (UWB) pulse utilizing the nonlinear dynamics of a semiconductor laser (SL). The output UWB chaotic optical pulses generated by the SL with optical feedback can be controlled when the feedback strength and driving current of the SL are tuned. Our experiment proves that the spectrum characteristics of the UWB pulses satisfy Federal Communications Commission regulations, and the experimental results are consistent with the simulated results based on the laser's rate equations.

Interfacial molecular assemblies of metalloporphyrins with two trans or one axial ligands.

Molecular assemblies of metalloporphyrins trans-dichloro(5,10,15,20-tetra-p-tolylporphyrinato)tin(IV) (SnCl2TPPMe) and trans-dihydroxo(5,10,15,20-tetra-p-tolylporphyrinato)tin(IV) (Sn(OH)2TPPMe), which have two trans axial ligands, as well 5,10,15,20-tetrakis(4-methoxyphenyl)-21H,23H-porphine iron(III) chloride (FeClTPPOMe) and 5,10,15,20-tetraphenyl-21H,23H-porphine manganese(III) chloride (MnClTPP), which have one axial ligand, are interfacially organized by Langmuir and Langmuir-Blodgett (LB) techniques. SnCl2TPPMe and Sn(OH)2TPPMe form nanofibrous structures which can display distinct supramolecular chirality, although the molecular units themselves are achiral, while FeClTPPOMe and MnClTPP form irregular nanoparticles that display negligible supramolecular chirality. An interpretation in terms of the effects of the axial ligands is proposed for this interesting phenomenon. Moreover, compared with assemblies of the diprotonated free-base porphyrins, which are fabricated by interfacial (air/2.4 M HCl) organization of free-base porphyrin, those of SnCl2TPPMe and Sn(OH)2TPPMe display higher stability in terms of supramolecular chirality. These results indicate that the assembly properties of metalloporphyrins can essentially be affected by the axial ligands that are attached to their chromophores, and that stable chiral porphyrin supramolecular associations can be easily produced by using achiral metalloporphyrins bearing two trans axial ligands.

Diastereoselective synthesis of chiral diporphyrins via intramolecular meso-meso oxidative coupling.

Diastereoselective syntheses of meso-meso linked diporphyrins were achieved via intramolecular chiral induction. The structures and conformations were analyzed by CD, UV, NMR, and computational calculations.

A novel soluble tin(IV) porphyrin modified single-walled carbon nanotube nanohybrid with light harvesting properties.

A dihydroxotin(IV) porphyrin functionalized single-walled carbon nanotubes (SWNTs) nanohybrid is obtained. Solubility of the nanohybrid in organic solvents is determined by UV-Vis-NIR absorption spectroscopy. Electron absorption and fluorescence spectra investigations demonstrate that efficient electron transfer occurs within the nanohybrid at the photoexcited state and the charge-separated state of the nanohybrid is observed by transient absorption spectrum. The results illustrate that this soluble electron donor-acceptor nanohybrid might be a good candidate as a light harvesting material in molecular photoelectronic devices.

Study on nonlinear spectroscopy of tetraphenylporphyrin and dithiaporphyrin diacids.

The nonlinear absorption of two porphyrin diacids (H4TPP2+ and H2DSP2+), the diprotonated forms of free base tetraphenylporphyrin (H2TPP) and dithiaporphyrin (DSP), were studied in the wavelength range of 500-650 nm. The two porphyrin diacids exhibited perturbed static and dynamic characteristics and enhanced nonlinear absorption properties relative to their parent neutral complexes in solution. Furthermore, for the dithiaporphyrin diacid, the introduction of S-atoms into the porphyrin core makes it a better candidate for optical limiting relative to the simple porphyrin. Their photophysical parameters such as ground and excited states absorption cross-sections, together with fluorescence lifetime and intersystem crossing time, were determined.

Active tuning of nonlinear absorption in a supramolecular zinc diphenylporphyrin-pyridine system.

We report on an active tuning of nonlinear absorption from reverse saturable absorption to saturable absorption in supramolecular zinc diphenylporphyrins by the combination of molecular and supramolecular levels at 532, 542 and 552 nm. Firstly, the modifications of molecular structures with bromination result in a discrete but regular change in magnitude and sign of nonlinear absorption (NLA). Furthermore, a fine tuning of NLA was obtained by the intermolecular weak interaction of pyridine and zinc porphyrins. Using an association model, we theoretically simulate the change of NLA. Compared with modifying molecular structures of conventional organic materials, the weak intermolecular interaction of supramolecular porphyrins has another advantage that it can be realized more easily and flexibly to change NLA.

Nonlinear absorption and nonlinear refraction of self-assembled porphyrins.

Nonlinear refraction and nonlinear absorption of self-assembled porphyrins in the nanosecond and picosecond regimes were studied at 532 nm by the Z-scan technique. First, a marked difference in nonlinear refraction was observed between self-assembled zinc porphyrins and free base porphyrins; however, the effects of self-assembly and metallization on nonlinear absorption are small. Second, an enhancement of nonlinear absorption was observed for the monomeric components of self-assembled structures by adding pyridine, while their nonlinear refractions remained almost unchanged as pyridine was added. It is expected that the metallization and addition of ligand can provide more convenient routes to alter the optical nonlinearities of porphyrins than the modifications of molecular structures of traditional covalent-bond organic materials.

DFT study on the geometric, electronic structure and Raman spectra of 5,15-diphenylporphine.

The ground state geometric, electronic structure and Raman spectra of 5,15-diphenylporphine (H(2)DPP) have been studied using B3LYP/6-31G(d) method and compared with that of well-studied free base porphine (H(2)P) and meso-tetraphenylporphine (H(2)TPP). Calculation shows that 5,15-substitution causes remarkable in-plane distortion, whereas the resulting out-of-plane distortion is negligible. The calculated electronic structure of H(2)DPP is consistent with the absorption spectra compared with H(2)P and H(2)TPP. The calculated vibrational frequencies of H(2)DPP scaled with a single factor of 0.971 agree well with experimental data (the rms error is 8.0 cm(-1)). The assignment of experimental Raman bands of H(2)DPP was discussed on the basis of theoretical calculation and the comparison with that of H(2)P and H(2)TPP. The splitting of some vibrational modes involving the motion of C(m) atom, such as nu(1), nu(8), and nu(10), was observed and was attributed to the diversification of the environment around C(m) atoms. As the shift of absorption peaks, the shift of some structure-sensitive Raman bands of H(2)DPP form that of H(2)TPP and H(2)P was attributed to the in-plane nuclear reorganization (IPNR) induced by phenyl-substitution, though the contribution of nonplanarity mechanism could not be excluded completely.

A meso-meso directly linked porphyrin dimer-based double D-π-A sensitizer for efficient dye-sensitized solar cells.

A novel double D-π-A branched dye () was synthesized and applied as a sensitizer for DSSCs. exhibited broader and stronger light absorption capability than the single D-π-A dye (). In the meantime, the orthogonal conformation of was found to be favorable for impeding intermolecular aggregation. Consequently, a power conversion efficiency of 5.33% was achieved under AM 1.5G conditions.

meso-2'-Linked porphyrin-BODIPY hybrids: synthesis and efficient excitation energy transfer.

Three meso-2'-linked porphyrin-BODIPY hybrids which contain one, two, and four BODIPY units (, , and ), respectively, were synthesized. Their photophysical properties were investigated by UV-vis and fluorescence spectroscopy, cyclic voltammetry, and femtosecond transient absorption spectroscopy, as well as by theoretical calculations. The electronic properties of the constituent chromophores were found to be largely retained in these hybrids. Meanwhile, efficient and rapid energy transfers from (1)* to were evaluated to be 1.2 × 10(11), 1.5 × 10(11), and 1.1 × 10(11) s(-1), respectively.

Benzo[a]carbazole-Based Donor-π-Acceptor Type Organic Dyes for Highly Efficient Dye-Sensitized Solar Cells.

A novel class of metal-free organic dyes based on benzo[a]carbazole have been designed, synthesized, and used in dye-sensitized solar cells for the first time. These types of dyes consisted of a cyanoacrylic acid moiety as the electron acceptor/anchoring group and different electron-rich spacers such as thiophene (JY21), furan (JY22), and oligothiophene (JY23) as the π-linkers. The photophysical, electrochemical, and photovoltaic properties, as well as theoretical calculations of these dyes were investigated. The photovoltaic performances of these dyes were found to be highly relevant to the π-conjugated linkers. In particular, dye JY23 exhibited a broad IPCE response with a photocurrent signal up to about 740 nm covering the most region of the UV-visible light. A DSSC based on JY23 showed the best photovoltaic performance with a Jsc of 14.8 mA cm(-2), a Voc of 744 mV, and a FF of 0.68, achieving a power conversion efficiency of 7.54% under standard AM 1.5 G irradiation.

[Effects of Zhuang-medical thread moxibustion combined with needle-pricking on vascular oxidative stress injury in the rat].

OBJECTIVE: To observe the effect of Zhuang-medical thread moxibustion combined with needle-pricking on vascular oxidative stress injury in oxidative stress injury rats. METHODS: Eighty Wistar rats were randomly allocated to normal control, sham operation (sham), model, and combined treatment groups (n=20 in each group). The oxidative stress injury model was established by ligation of the left sciatic nerve to induce chronic constriction injury (CCI) pain stress stimulation. Zhuang-medical thread moxibustion was applied to bilateral "Zusanli" (ST 36), once a day for 3 weeks. Needle-pricking was applied to left "Yanglingquan" (GB 34) and left "Huantiao" (GB 30), once a day for 3 weeks except Sundays. Plasma 6-keto-PGF 1α, thromboxane B 2 (TXB 2), NO and ET contents were assayed by radioimmunoassay. COX-2 immunoactivity of the femoral artery was determined by immunohistochemistry, and pathological changes of the femoral artery were detected by H. E. staining. RESULTS: Compared with the control group, the levels of plasma 6-keto-PGF 1α and NO in the model group were significantly reduced (P<0.05), while those of plasma TXB 2 and ET and COX-2 expression in the femoral artery were obviously increased in the model group (P<0.01). After moxibustion plus needle-pricking treatment, CCI-induced decrease of plasma 6-keto-PGF 1α and NO contents, and increase of plasma TXB 2 and ET and COX-2 expression levels were obviously reversed (P<0.05, P<0.01). The tubal wall of the femoral artery in rats of the model group got thicker, while that of the combined treatment group was relatively thinner, suggesting an inhibition of vascular intimal hyperplasia after the treatment. CONCLUSION: Zhuang-medical thread moxibustion combined with needle-pricking of ST 36, GB 34 and GB 30 can reduce the expression of femoral artery COX-2 and regulate the balance of both plasma PGI 2/TXA 2 and plasma NO/ET in CCI-induced oxidative stress rats, which may contribute to its effect in suppressing oxidative stress-induced vascular intimal hyperplasia.