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With the purpose to develop long chain-conjugated oligopyrrin-like compounds and their metal complexes, and thus achieve tunable near-infrared absorption, a dithienyl-blocked hexapyrrane S2-P6 was synthesized by acid-catalyzed [2+4+2] condensation, followed by oxidation with DDQ to afford dithiaoctapyrrin 1, and its mononuclear metal complexes 1-Cu and 1-Zn were synthesized by treating 1 with Cu(II) and Zn(II) acetates. All the compounds were systematically characterized by NMR/EPR, and HRMS. The crystal structures revealed that 1 adopts a double hook-like conformation. Whereas, both complexes 1-Cu and 1-Zn adopt spiral-hook hybrid conformations, showing smaller interplanar angles between the rings within the spiral part, compared with those in the hook-like counterpart of molecule 1, which is favorable for red-shifting the absorption. As expected, the absorption band edges for complexes 1-Cu and 1-Zn are red-shifted to ca. 1560 nm, compared with that of 1260 nm observed for 1.

Donor-linked concerted companion dyes have been synthesized for fabricating solar cells. The results indicate that a longer linking chain is favorable for improving the proportion of double anchoring, resulting in superior photovoltaic performance.

A hexapyrrane P6 with a terminal N-confused pyrrole was synthesized by acid-catalyzed [3+3] condensation followed by oxidation with DDQ, which did not afford the expected N-confused hexaphyrin. In stead, a rearranged product, i.e., [Formula: see text]-dipyrrin appended N-confused porphyrin 1 was obtained in a yield of 46%. Chelation of 1 with Pt(II) afforded the peripheral complex 1-Pt, which was further coordinated with Rh(I) in the cavity to afford the corresponding bimetallic complex 1-Pt-Rh. Both 1-Pt and 1-Pt-Rh exhibit split Soret-like bands and noticeable Q-like bands tailing to the NIR region up to ca. 1200 nm. Single crystal X-ray diffraction analyses of 1 and 1-Pt revealed that the peripheral coordination of Pt(II) slightly modifies the interplanar angle between the porphyrin macrocycle and the dipyrrin unit, which may modulate the absorption spectra. The results of this work compose an interesting example of synthesizing porphyrinoids appended with conjugated peripheral chains by the oxidative ring closure reaction of an oligopyrrane containing a terminal N-confused pyrrole, and such compounds may be used for both inner and peripheral coordination to afford complexes with tunable NIR absorption.

Sulfolenopyrrole-based normal and N-confused phlorins have been constructed to address the seldom touched phlorin functionalization and simultaneously explore the effect of the pyrrole linkage modes (αα, αβ) on the [4 + 2] cycloaddition reaction. The common sulfolenophlorin

Introduction of a dialkoxy-substituted tetraphenylethylene entity into porphyrin sensitizers improves the photovoltages and efficiencies of dye sensitized solar cells, affording a high power conversion efficiency of 12.3%.

Sapphyrin is a pentapyrrolic expanded porphyrin with a 22π aromatic character. Herein, we report the synthesis of a 20π antiaromatic sapphyrin isomer 1 by oxidative cyclization of a pentapyrrane precursor P

Concerted companion dyes (CC dyes) like XW61 have been demonstrated to be an effective platform for developing efficient DSSCs. However, the moderated phenothiazine-based electron donor in XW61 results in unsatisfactory Jsc. To address this problem, a stronger fluorenyl indoline-based electron donor has been used to construct porphyrin dye XW68 and organic dyes Y1-Y2. The stronger electron-donating character of the fluorenyl indoline unit leads to an enhanced Jsc value (20.48 mA·cm-2) for the individual dye XW68. On this basis, CC dyes XW69-XW70-C8 have been designed and synthesized by combining the frameworks of Y1 and Y2 with XW68. The complementary absorption characters of the porphyrin and the organic dye moieties lead to panchromatic absorption with a strong light-harvesting capability from 350 to 700 nm and the onset wavelength extended to ca. 840 nm in the IPCE curves. As a result, excellent Jsc values have been achieved (>22 mA·cm-2). In addition to the advantages of high Jsc, bulky octyl groups have been introduced into the donor of XW70-C8 to reduce dye aggregation and suppress charge recombination. Finally, a highest PCE of 11.1% with a satisfactory Jsc (22.25 mA·cm-2) and an enhanced Voc (750 mV) has been achieved upon coadsorption of XW70-C8 with CDCA. In addition, the CC dye XW70-C8-based solar cells exhibit excellent long-term photostability. These results provide an effective method for rationally improving the photovoltaic behavior, especially the Jsc of CC dyes, by introducing strong electron donor moieties with suitable substituents.

A doubly confused thiapentapyrrane NSP-5 was synthesized by acid-catalysed condensation. Subsequent oxidation with DDQ did not afford the expected thiasapphyrin-like product. Instead, two tetrapyrrolic macrocycles, i.e. neo-N-confused phlorin (1) and N-confused phlorin-II (2) were obtained in the yields of 14% and 18%, respectively. The compounds were characterized by NMR, HRMS, and X-ray diffraction analyses. Single crystal structures clearly reveal that the thienyl units are not embedded into the macrocycles, but appended as meso-substituents, and the C[Formula: see text]-N and C[Formula: see text]-C[Formula: see text] cyclization modes can be clearly revealed by the crystal structures of 1 and 2, respectively. The observation that the thienyl unit is not involved in oxidative cyclization may be related to the relatively low reactivity of the thiophene moiety compared with the more electron-rich pyrrole unit. These results indicate that oxidative cyclization of linear thiaoligopyrranes containing terminal thiophene units may be developed as an effective approach for synthesizing nonconjugated macrocycles like phlorin analogues.

To develop efficient dye-sensitized solar cells (DSSCs), concerted companion (CC) dyes

In this work, organic concerted companion (CC) dyes CCOD-1 and CCOD-2 were constructed by covalently linking two organic dye units with complementary absorption spectra. Both CC dyes exhibited intense absorption from 300 to 650 nm with the band edges extended to 700 nm. These CC dyes were used to fabricate dye-sensitized solar cells (DSSCs), and the photovoltaic performance was investigated using different light sources. CCOD-2 possessed bulkier outer shelter than CCOD-1 owing to the longer carbon chains (C

Tandem Diels-Alder reactions of masked porphyrindienes (i.e., sulfolenoporphyrins) with benzoquinones and stilbenes, followed by aromatization, have been developed to load porphyrin with mixed annulation units (i.e., terphenyl and naphthoquinone), furnishing the low-symmetry π-extended porphyrins (

A facile synthetic strategy towards conformationally stable chiral chromophores based on dimeric porphyrinoids has been established. A peculiar class of face-to-face intramolecularly interlocked corrole dimers were formed by the oxidative C-C coupling linked at the inner carbon sites upon simple treatment of copper(II) ions. Their intrinsic electronic structures were modulated by the peripheral corrole ring annulations, which lead to distinct optical properties and redox profiles. The stereogenic carbon centers implemented in the confused corrole skeleton provided a rationale for designing novel chiral materials.

Tetracenequinone fused porphyrin Ni4TQ has been synthesized and the long tetracenequinone units at the vertices of porphyrin exhibit an intense π,π-interaction, which can be regulated by solvents to furnish different shapes of crystals or various uniform flower-shaped biomorphs.

To fabricate efficient dye-sensitized solar cells (DSSCs), 4-tert-butylpyridine (TBP) is commonly used as an additive in the electrolytes for improving the photovoltages (VOC). However, TBP cannot play a positive role in improving the photocurrent (JSC) because of the lack of absorption in the visible-wavelength range. We herein report a light-absorbing pyridine derivative N1 as an additive for the axial coordination with porphyrin dyes. N1 was synthesized by introducing a (bis(4-methoxyphenyl)amino)anthryl moiety into the para-position of pyridine via an acetylene bridge, and porphyrin dye XW64 containing meso-3,5-disubstituted phenyl groups was synthesized considering that the meta-substituted phenyl groups may induce weaker steric hindrance with the axial pyridyl ligand, as compared with wrapped and strapped porphyrin dyes. Thus, N1 was used as an electrolyte additive together with TBP. When optimized concentrations of 6 mM N1 and 0.5 M TBP were used for fabricating DSSCs based on XW64, enhanced photovoltaic performance was achieved, with JSC, VOC, and efficiency of 15.65 mA·cm-2, 0.701 V, and 7.35%, respectively, superior to those of the corresponding DSSCs without using the additives (JSC = 14.86 mA·cm-2, VOC = 0.599 V, and efficiency = 5.94%). The enhancement of JSC can be ascribed to the improved light-harvesting ability induced by the axially coordinated N1. Furthermore, the two additives also can be used to fabricate efficient solar cells based on the wrapped porphyrin dye XW42, achieving high efficiency of 10.3%, indicative of their general applicability in fabricating high-performance DSSCs. These results indicate that the simultaneous employment of the traditional TBP additive and a pyridyl ligand with light-harvesting ability in the electrolyte for the axial coordination to a porphyrin dye is a promising approach for developing efficient DSSCs.

An N-confused hexapyrrolic phlorinoid 1 and its isomer N-fused hexapyrrolic phlorinoid 2 were synthesized through [4 + 2] condensation. Both 1 and 2 can be readily transformed into N-confused hexapyrrolic phlorinone 3 under aerobic conditions. Coordination of 1 with Cu(acac)2 afforded two different mono-Cu(II) complexes 4 and 5 with CNNN and ONNN coordination environments, respectively. The NIR absorption bands can be effectively modulated up to 1265 nm through the oxidation, fusion, and metalation reactions.

Novel interrupted π-conjugated macrocycles derived from expanded porphyrinoids were synthesized, and their unique reactivity was investigated in this work. The specific porphyrin analogs, so-called phlorins and isoporphyrins, possess a meso-sp3 methylene moiety, showing inner 3NH and 1NH pyrrolic cores, respectively, and extended near-infrared (NIR) absorption. Expanded N-confused pentapyrrolic phlorin analog 1 bears an interrupted cyclic π-conjugated system that is featured by a distinct higher HOMO and a lower LUMO. Oxidation of 1 allowed structural transformations through the expanded isoporphyrin-like species 2. One of the representative products is a spiro-carbon-bridged multiply N-fused product 3 comprising a fused [5.6.5.7.6.5]-hexacyclic ring obtained by oxidation with 2,3-dichloro-5,6-dicyano-p-benzoquinone. When magic blue was used as the oxidant, an aromatic N-confused pentaphyrin 4 was obtained via migration of one of the meso-phenyl groups to the β-position of the neighboring pyrrolic ring. By employing the flexible cavity of 1 for metal coordination, Pd(II) complexation occurred with a specific meso oxygenation to give a bimetallic complex 5. In contrast to the rich oxidation reactions, reduction of 1 with NaBH4 resulted in the regioselective nucleophilic hydrogen substitution reaction at the para position of one of the meso-C6F5 groups. These results provide a practical approach for synthesizing novel interrupted or aromatic π-conjugated frameworks showing NIR absorptions.

To achieve high power conversion efficiency (PCE), three porphyrin sensitizers have been synthesized and explored to simultaneously enhance the photocurrent (Jsc) and photovoltage (Voc). On basis of the XW4, a benzothiadiazole (BTD) unit has been introduced to afford XW57 with the aim to extend the absorption wavelength and enhance the light harvesting ability. As a result, a Jsc of 13.72 mA/cm2 has been obtained for XW57, higher than that of XW4. On this basis, XW58 has been prepared by modifying the carbazole-based donor with two bulky dihexyloxyphenyl groups, and the superior anti-aggregation character raises the Voc from 781 mV (XW4) to 844 mV. When both the BTD unit and the bulky groups are introduced to the acceptor and donor units, respectively, the resulting sensitizer XW59 exhibits a highest PCE value of 7.34% with synergistically enhanced Jsc of 13.19 mA/cm2 and Voc of 793 mV. These results provide further insight into developing high performance dye-sensitized solar cells

Oxidation of a thiophene-hexapyrrane hybrid S-P6 afforded a stable conjugated open-chain thiaheptapyrrolic helix 1 with the terminal thiophene and confused pyrrole units lying at a long distance that is adverse for further cyclization. Chelation of 1 with copper(II) ion afforded 1-Cu, which exhibits more distant terminal units. Interestingly, further oxidation of 1 triggered an intramolecular C-N fusion reaction to afford a unique 5,5,5-tricyclic fused linear thiaheptapyrrin 2, with the two terminals positioned in proximity, which favors the oxidative ring-closure reaction to give a unique 5,5,5-tricyclic fused thiaheptaphyrin (1.1.1.1.1.1.0) 3 under air. The inner-fusion strategy for positioning the reactive sites in proximity to promote oxidative cyclization offers a new approach for constructing large porphyrinoids through conjugated oligopyrrins without the assistance of metal ions.

With the purpose to achieve panchromatic absorption for constructing efficient dye-sensitized solar cells (DSSCs), the cosensitization approach of using two dyes with complementary absorption has been developed with great success. However, this approach usually requires time-consuming optimization of a number of parameters for controlling the ratio and distribution of the two coadsorbed dyes on TiO2 film, which limits the potentials of this strategy. We herein report an alternative approach for developing efficient DSSCs by designing a class of "concerted companion dyes" with two complementary dye components linked covalently. Thus, a newly synthesized organic dye Z2 was linked to a recently reported doubly strapped porphyrin dye XW51 through flexible chains with various lengths to afford XW60-XW63. These dyes exhibit excellent absorption and efficiencies in the range of 8.8%-11.7%. Notably, upon coadsorption with chenodeoxycholic acid, XW61 affords an impressive efficiency of 12.4%, a record for iodine electrolyte-based DSSCs, to the best of our knowledge. In addition, these dyes also exhibit the advantages of easy cell fabrication, simple optimization, as well as excellent photostability.

Porphyrin dyes have been widely used for the fabrication of efficient dye-sensitized solar cells (DSSCs). However, dye aggregation and charge recombination still exert negative effects on photovoltaic performance, resulting in unsatisfactory power conversion efficiencies (PCEs). Herein, we report a new class of porphyrin sensitizers, XW52 and XW53 employing four benzyloxy groups to wrap the porphyrin cores. As a result, an efficiency of 7.6% was obtained for XW52, with [Formula: see text] and [Formula: see text] of 668 mV and 16.63 mA cm[Formula: see text], respectively. Compared with XW52, an additional 2,6-dialkoxyphenyl group has been introduced to the N-atom of the phenothiazine donor to furnish XW53 with the aim to further improve the anti-aggregation character and the solubility, and thus the [Formula: see text] was improved to 674 mV, and a higher efficiency of 7.9% was achieved for XW53. Upon cosensitization with PT-C6, the[Formula: see text] and [Formula: see text] were synergistically enhanced to 727 mV and 18.67 mA cm[Formula: see text], respectively. As a result, a high efficiency of 9.6% was successfully achieved for the cosensitization system of XW53 + PT-C6. These results provide an effective novel strategy for designing efficient porphyrin dyes by introducing multiple benzyloxy groups to the meso-phenyl groups.

Dye-sensitized solar cells (DSSCs), as a cost effective and eco-friendly photovoltaic technology for utilizing solar energy, are promising in meeting the increasing demand of clean and renewable energy resources. Among various sensitizers, porphyrins are crucial candidates with the advantages of strong absorption in a wide spectral range, tunable photophysical and electrochemical properties, and long-lived excited states facilitating electron injection. After decades of development, the power conversion efficiencies of porphyrin-based DSSCs have exceeded 13%, showing the great potential of porphyrins in fabricating highly efficient DSSCs. This review summarizes effective molecular engineering strategies for optimizing porphyrin sensitizers as well as intermolecular engineering of coadsorption and cosensitization systems, with the aim to provide further insight into the molecular structure–photovoltaic performance correlations and an outlook on possible exploration directions in the future for achieving DSSCs with high efficiencies, long-term stability and low cost feasible for practical applications. In addition, the recent advances of porphyrin-based organic solar cells (OSCs) are briefly introduced considering similar design strategies employed for developing porphyrin dyes for DSSCs and active materials for OSCs.

An N-confused phlorin isomer bearing a dipyrrin moiety at the α-position of the confused pyrrole ring (1) was synthesized. PdII and BIII coordination at the peripheral prodigiosin-like moiety of 1 afforded the corresponding complexes 2 and 3. Reflux of 2 in triethylamine (TEA) converted the meso-phenyl into the PdII -coordinating phenoxy group to afford 4. Under the same reaction conditions, TEA was linked to the α-position of the dipyrrin unit in 3 as an N,N-diethylaminovinyl group to afford 5. Furthermore, peripheral coordination of BIII in 3 and 5 improved the planarity of the phlorin macrocycle and thus facilitated the coordination of AgIII at the inner cavity to afford 3-Ag and 5-Ag, respectively. These results provide an effective approach for developing unique porphyrinoids through peripheral coordination.

A corrorin parasitized hexaphyrin(1.1.1.1.1.0) 1 was synthesized by [4 + 4] condensation, and subsequent treatment with PbO2 afforded hexaphyrin 2 appended with a dipyrrinone moiety via regioselective opening of the corrorin ring. In contrast, oxidation of the corresponding corrorin-N-confused hexaphyrin(1.1.1.1.1.0) hybrid 3 afforded only a keto adduct 4. As a result, the planarity and aromaticity of the hexaphyrin moiety can be modulated.

Three new porphyrin dyes XW45 − XW47 have been synthesized employing a dialkoxy-wrapped phenothiazine donor, a tetraalkoxy-wrapped porphyrin π-framework, a benzothiadiazole (BTD)-based auxiliary acceptor, and an anchoring benzoic acid group. On the basis of our previously reported dye XW36 , XW45 was synthesized by introducing a BTD unit to broaden the absorption spectrum, further introducing a hexyl-substituent into the BTD unit afforded XW46 , and an additional fluorine atom was introduced to the carboxyphenyl acceptor to afford XW47 . As expected, the BTD unit obviously broadens and red-shifts the absorption threshold of XW45 − XW47 to ca . 750 nm. Dye-sensitized solar cells (DSSCs) were fabricated based on a cobalt electrolyte using chenodeoxycholic acid (CDCA) as the coadsorbent. Under full sun illumination, XW45 exhibits an efficiency of 9.73%, which is slightly lower than that of 10.19% obtained for the reference dye SM315 . By contrast, XW46 and XW47 show higher efficiencies than SM315 owing to the improved anti-aggregation ability associated with the hexyl group on the BTD unit and better ICT effect induced by the fluorine atom on the carboxyphenyl unit. Thus, XW47 exhibits the highest efficiency of 10.41% among the porphyrin dyes. Furthermore, PT-C6 was used as the cosensitizer to improve the light harvesting ability and efficiencies of the cells due to its broad absorption within 350–560 nm. Thus, high efficiencies of 10.32%, 11.38% and 10.90% were achieved for the cosensitized solar cells based on XW45 – XW47 , respectively, owing to the obviously enhanced photocurrent density ( J SC). In addition, under 30% full sun illumination, XW46 + PT-C6 exhibits a high efficiency of 13.08%. These results give an effective method for building high performance DSSCs through the cosensitization of porphyrin dyes containing a wrapped donor, a wrapped porphyrin framework and a properly substituted auxiliary benzothiadiazole unit.

A hybrid thia-norhexaphyrin comprising a directly linked N-confused pyrrole and thiophene unit (1) revealed unique macrocycle transformations to afford multiply inner-annulated aromatic macrocycles. Oxidation with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone triggered a cleavage of the C-S bond of the thiophene unit, accompanied with skeletal rearrangement to afford unique π-conjugated products: a thiopyrrolo-pentaphyrin embedded with a pyrrolo[1,2]isothiazole (2), a sulfur-free pentaphyrin incorporating an indolizine moiety (3), and a thiopyranyltriphyrinoid containing a 2H-thiopyran unit (4). Furthermore, 2 underwent desulfurization reactions to afford a fused pentaphyrin containing a pyrrolizine moiety (5) under mild conditions. Using expanded porphyrin scaffolds, oxidative thiophene cleavage and desulfurization of the hitherto unknown N-confused core-modified macrocycles would be a practical approach for developing unique polypyrrolic aromatic macrocycles.

A series of new porphyrin dyes (XW42-XW44) containing oligo(ethylene glycol) units have been designed and synthesized. Two triethylene glycol units were introduced into the phenothiazine moiety of XW42, whereas diethylene glycol (DEG) and ethylene glycol chains were introduced to afford XW43 and XW44, respectively. Interestingly, the efficiencies of the DSSCs were clearly dependent on the chain lengths. Among the three dyes, XW42 and XW43 exhibited relatively high open-circuit voltages of 751 and 750 mV, respectively, and XW43 exhibited the highest efficiency of 10.32 % owing to the presence of the DEG chains with suitable lengths and excellent ability to trap Li+ . Furthermore, through a combined coadsorption and cosensitization approach, the efficiencies were dramatically enhanced. As a result, a highest efficiency of 12.10 % was obtained for the XW43+chenodeoxycholic acid+PT-C6 (a metal-free organic dye) system, which ranks among the highest efficiencies of cells based on the traditional iodine electrolyte.

Four novel porphyrin dyes XW48–XW51 with a doubly strapped porphyrin framework and judicious optimization of the substituents of the phenothiazine donor have been synthesized and utilized as DSSC dyes. On the basis of XW40, bulky 2,6-bis(hexyloxy)phenyl groups were incorporated into the phenothiazine donor by replacing the hexyl, 4-hexyloxyphenyl and both of them, to afford XW48, XW49 and XW50, respectively. On the basis of XW50, XW51 was synthesized by using 2,4-bis(hexyloxy)phenyl in place of the 2,6-bis(hexyloxy)phenyl units. As a result, the Voc values were enhanced stepwisely from 730 mV (XW40) to ca. 750 mV (XW48/XW49) and then to 761 mV (XW50). Compared with XW50, XW51 contains a bulky donor with more evenly distributed alkoxyl chains, which tend to form a more compact self-assembled monolayer to impede the penetration of I3−. Hence, an extraordinarily high Voc of 781 mV was achieved for XW51. As a result, the efficiency was dramatically improved to 11.1%, which is the highest efficiency for DSSCs based on an individual sensitizer using the iodine electrolyte, to the best of our knowledge. Furthermore, high efficiencies of 10.1% and 9.7% were also obtained for XW50 and XW51, respectively, based on the cobalt electrolyte.

Porphyrin sensitizers play essential roles in the development of efficient dye-sensitized solar cells (DSSCs). To further improve power conversion efficiency (PCE), it is vital to reduce undesirable dye aggregation that causes serious charge recombination and lowered open-circuit voltages (Voc). To this end, we herein report a new class of porphyrin-based dyes XW40 and XW41, with the porphyrin cores strapped with two circle chains. Compared with the reference sensitizer XW10 which contains a porphyrin core wrapped in four dodecoxyl chains, the double strapping in XW40 not only effectively suppresses the dye aggregation but also improves the dye loading amount. As a result, the Voc and photocurrent (Jsc) were improved by 19 mV and 0.8 mA cm−2, respectively, compared with the corresponding values of XW10, and the efficiency was improved from 8.6% obtained for XW10 to 9.3% for XW40. To further extend the spectral response, an electron-withdrawing benzothiadiazole (BTD) unit was introduced as an auxiliary acceptor in XW41. Impressively, the onset wavelength of its IPCE spectrum was dramatically red-shifted to 830 nm. However, the extended π-conjugation framework results in aggravated dye aggregation, and thus a lowered efficiency of 8.2% was obtained for XW41. Through a combined approach of coadsorption and cosensitization, the efficiencies were dramatically enhanced to 10.6% and 10.2% for XW40 and XW41, respectively, as a result of simultaneously enhanced Voc and Jsc. The results of this work provide a novel strategy for developing efficient DSSCs by employing strapped porphyrin dyes.

Directly linked porphyrin dimers have attracted considerable attention because of their intriguing electronic features. Most emphasis has been placed on either dimers with large dihedral angles between the constituent planar monomeric subunits or those with overall planarity, referred to as “Planar-Twisted-Planar” and “Planar-Planar-Planar”, respectively. Herein, we report a “Twisted-Planar-Twisted” framework, the hexaphyrin dimer D that exists in a trans configuration. Treatment of D with MeOH affords two isomeric dimers, MD1 and MD2, both of which incorporate a methoxy moiety and exist in cis orientations with respect to the tethering linkage. The methanol-promoted conversion is accompanied by a readily discernible color change from green to brown and is not induced to an appreciable level by other alcohols. Dimer D thus acts as a rudimentary, albeit highly selective, reaction-based methanol indicator. This work provides a promising approach for constructing reaction-based chemosensors using porphyrinoid dimers of nonplanar subunits with biased reactivity., Directly linked porphyrin dimers show intriguing electronic features but emphasis has been placed on planar monomeric units. Here, the authors report a Twisted-Planar-Twisted framework which can undergo a cis-trans transformation accompanied by a colour change in presence of methanol, making this framework applicable as a methanol sensor.

Oxidative ring closure of linear oligopyrroles is one of the synthetic approaches to novel porphyrinoids with dinuclear coordination sites and helical chirality. The spatial arrangement of the pyrrolic groups of octapyrrole (P8) affected the position of the intramolecular oxidative coupling of the pyrrolic units; tripyrrin-armed isosmaragdyrin analogue (1) containing a β,β-linked bipyrrole moiety was synthesized regioselectively in a high yield by using FeCl3. NiII-coordination at the armed tripyrrin site of 1 allowed the formation of diastereomeric helical twisted complexes (2A and 2B) and succeeding CuII-coordination at the macrocyclic core afforded heterodinuclear NiII/CuII-complexes (3A and 3B). Each of them comprised a pair of separable enantiomers, exhibiting P- and M-helices, respectively. Notably, diastereomeric interconversion from 2A to 2B was quantitatively achieved as a consequence of helical transformation under acidic conditions., A tripyrrin-armed isosmaragdyrin containing a β,β-linked bipyrrole moiety has been synthesized from a linear octapyrrole, and the succeeding metallation afforded an enantiomer pair of mononuclear NiII- and heterodinuclear NiII/CuII-complexes that exhibit P- and M-helices.

The recently synthesized twisted thia-norhexaphyrin and its multiply annulated polypyrrolic derivatives have been studied computationally. Gauge-including magnetically induced current calculations predict a global nonaromatic character of the initial thia-norhexaphyrin due to the highly-twisted conformation of the macrocycle. Upon the oxidation of the thia-norhexaphyrin the four multiply annulated polypyrrolic aromatic macrocycles are formed for which the global aromatic character is confirmed in agreement with experimentally measured 1H NMR spectra. The calculations of the proton chemical shifts for the studied compounds by direct comparison with the tetramethylsilane standard leads to a significant mean absolute error. At the same time a linear regression procedure for the two selected groups of protons (CH and NH protons) provides much better values of calculated chemical shifts and tight correlation with experiment. The separate consideration of NH protons is motivated by the numerous intermolecular hydrogen bonds in which the protons are involved that induce considerable upfield shifts leading to the significant underestimation of corresponding chemical shifts. Such a selected correlation can be used for accurate estimation of proton chemical shifts of the related porphyrinoids. Bader's theory of Atoms in Molecules has been applied for the studied twisted thia-norhexaphyrin and its multiply annulated polypyrrolic derivatives to characterize the intramolecular H-bonds and other non-covalent interactions.

A doubly SO2-fused phlorin 4 has been synthesized by the [2 + 2] condensation of dipyrromethanecarbinol 2 and SO2-fused dipyrromenthane 3 in the presence of TFA, followed by DDQ oxidation. The SO2-fused phlorin 4 has been characterized by absorption, fluorescence, mass and NMR spectra, as well as X-ray analysis. Compared to the [Formula: see text]-unsubstituted phlorin 5, the SO2-fused phlorin 4 exhibits a red-shifted absorption spectrum (around 12 nm), a more distorted molecular conformation, as well as nice photostability even with an electron-donating meso-3,5-di-tert-butylphenyl group. The titration of 4 and 5 with TBAF has been monitored by absorption spectroscopy. The deprotonated phlorin 4 shows a peak at 870 nm which is red shifted by 26 nm compared to that of deprotonated 5.

Dye-sensitized solar cells (DSSCs) have attracted intensive attention in developing photovoltaic devices for employing solar energy. For developing panchromatic and efficient porphyrin sensitizers, it has been demonstrated to be an effective approach to introduce an electron-withdrawing benzothiadiazole unit as an extra electron acceptor. In contrast, the structurally similar benzotriazole moiety remains relatively unknown in this respect. In this work, we have synthesized a novel porphyrin dye containing an extra electron acceptor of benzotriazole. Photophysical and electrochemical investigations revealed red-shifted absorption and a narrower band gap induced by the benzotriazole unit. Thus, a reasonable efficiency of 8.39% has been achieved with a Jsc of 17.00 mA cm−2 and a Voc of 712 mV. On this basis, to investigate the effect of the dihedral angle between the benzotriazole and the adjacent phenylene ring, one or two methyl groups were attached to the ortho-positions of the phenylene ring. As a result, the enlarged torsion angles induce poor electronic coupling between the LUMO of the dyes and TiO2, resulting in lower efficiencies of 6.61% and 3.62%, respectively. With the purpose to further improve the efficiencies, coadsorption and cosensitization approaches were employed. And the efficiencies have been successfully elevated to 9.32%, 8.49% and 7.34%, respectively. These results demonstrate the effectiveness of incorporating an auxiliary benzotriazole acceptor into porphyrin dyes on achieving extended light-harvesting wavelength ranges and illustrate the importance of avoiding severe torsion within the acceptor part of the porphyrin dyes. In contrast to the commonly used cosensitizers with absorption peaks lying in the absorption valley between the Soret band and the Q bands of porphyrin dyes (500–600 nm), the utilization of an organic dye with broad absorption in this work has been demonstrated to be effective for improving the efficiencies despite the fact that its absorption peak at 450 nm largely overlaps with the Soret band of the porphyrin dyes. These results provide an alternative approach for developing cosensitizers for porphyrin dyes.

Biothiols such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH) play vital roles in various physiological and pathological processes. In this work, a BODIPY-based fluorescent probe XCN was synthesized from multi-step reactions. We first synthesized a BODIPY derivative with a cyano and a bromine moiety attached to the 8-diphenylaminophenyl substituent of BODIPY, followed by the reaction with p-aminothiophenol under basic condition. Interestingly, compound XCN was successfully obtained with the p-aminophenylthio moiety introduced into one of the α-positions of the pyrrolic units. This reaction may compose an efficient approach for synthesizing novel BODIPY derivatives with substituents attached to the pyrrolic unit without previously brominating it. XCN can be used as a fluorescence turn-on probe to selectively detect Cys and Hcy using the cyano group as the recognition site, with the p-aminophenylthio moiety left unreacted. XCN was found to be nearly nonfluorescent, and it exhibits only slight fluorescence enhancement when treated with GSH. However, upon interaction with Cys or Hcy, the fluorescence was enhanced by 1081 and 1126 folds, respectively. In addition, XCN exhibits good selectivity and sensitivity towards Cys and Hcy over GSH and other amino acids in a wide pH range from 2 to 10 in aqueous buffers. Furthermore, XCN was successfully used for imaging biothiols in living A549 lung cancer cells.

Biothiols, such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH), play essential roles in many physiological and pathological processes. In this work, three porphyrin derivatives, XQ1 , XQ2 and XQ3 , were synthesized by combining the porphyrin framework with nitroethylene, bis(methoxycarbonyl)ethylene and dicyanoethylene moieties, respectively. XQ1 was almost nonfluorescent, which could be utilized as a good starting point for developing fluorescence turn-on probes. Thus, XQ1 exhibits fast fluorescence enhancement and high selectivity towards the biothiols based on the Michael addition mechanism. It also exhibits high sensitivity towards the biothiols with the detection limits of 0.65–1.1 μM. In addition, XQ1 was successfully applied to cell imaging in living A549 cells for visualizing the biothiols. The results compose a good example of designing porphyrin derivatives for detecting biothiols, with the advantages of dramatic fluorescence enhancement in the NIR wavelength range, which exhibits good cell membrane permeability and practicability in detecting both exogenous and endogenous biothiols.

In the past decades, porphyrin analogues have attracted increasing attention in light of their unique properties and potential applications in various areas. In this work, novel nonconjugated thiophene-embedded N-confused homoporphyrins 1 and 2 as well as a fully-conjugated N-fused homoporphyrin 3 have been prepared through acid-catalyzed condensation reactions followed by oxidation. Both 1 and 2 comprise two meso-sp3-carbon atoms. However, they are insensitive to the air or common oxidants. Single crystal X-ray diffraction analysis reveals that 2 adopts a highly distorted boat-like conformation, with the NH moieties of two pyrrolic units pointing outwards and an O atom attached to the α position of the N-confused pyrrole unit. As a result, hydrogen-bonded dimers are formed through the intermolecular hydrogen bonds between the lactam-like moieties. In contrast to the highly distorted structure of 2, N-fused homoporphyrin 3 contains a unique 5,5,5–tricyclic fused ring, and thus demonstrates a relatively coplanar conformation except one inverted pyrrole unit. Because of the different structural characters, 3 exhibits F− binding behavior distinct from that of 1 and 2.

Two fluorescence “turn-on” Zn2+ probes were developed by introducing an anthracenyl fluorophore through the linkage of a diphenylamino moiety at the 5-position of a dipyrrin moiety. Thus, two compounds with weak fluorescence were designed, synthesized, and employed as CHEF (chelation enhanced fluorescence) type fluorescence “turn-on” Zn2+ probes, which exhibit dramatic fluorescence enhancement upon addition of Zn2+, showing high sensitivities and impressive detection limits of 13 and 12 nM, respectively, better than their analogues containing simple aryl substituents at the 5 positions of a di- or tripyrrin moiety. In addition, both of the probes exhibit good selectivity, short response time of less than 10 s and wide applicable pH ranges. Furthermore, the weak fluorescence nature of the probes was rationalized based on viscosity dependence measurements and theoretical calculations. These results provide further insight into the development of selective and sensitive zinc probes.

The selective and sensitive detection of zinc ions has been an important research topic because of the vital role played by zinc ions in numerous physiological activities, and fluorescent probes have emerged as effective and powerful tools for zinc detection because of their simplicity andcereal-time monitoring nature. In this work, with the purpose to improve the binding affinities and sensitivities of dipyrrin based fluorescent Zn 2+ probes, strongly coordinating pyridyl moieties were introduced into dipyrrins. Aroylation of 5-pentafluorophenyl and 5-unsubstituted dipyrromethanes with picolinoyl chloride afforded two corresponding dipicolinoyl dipyrromethanes, which were further oxidized with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (DDQ) to afford the expected 5-pentafluorophenyl-substituted dipicolinoyl dipyrrin and a unique unexpected dipicolinoyl dipyrrolyl ketone, respectively. Both of these compounds exhibited noticeable fluorescence “turn-on” responses specifically to Zn 2+ over other metal cations, with fluorescence enhancements of 87 fold and 119 fold, respectively. However, because of the different substituents at the 5 positions and the different conjugation frameworks, distinct Zn 2+ sensing behavior was observed. For the 5-pentafluorophenyl-substituted dipicolinoyl dipyrrin, the sensing of Zn 2+ induced a color change from light orange to pink accompanied with enhanced red fluorescence. Whereas, the sensing of Zn 2+ by the dipicolinoyl dipyrrolyl ketone induced the color change from nearly colorless to bright yellow and enhanced green fluorescence. Based on high binding affinities and the dramatic spectral responses, both of the probes exhibit high sensitivities towards Zn 2+ with detection limits of 9.8 nM and 6.3 nM, respectively. In addition, fast responses within 10 s and wide applicable pH ranges are indicative of their potential applications as promising zinc probes. Finally, the 5-pentafluorophenyl dipicolinoyl dipyrrin was successfully applied to cell imaging in Hela cells, demonstrating its practical applicability. It is noteworthy that the single crystal structure of a Zn 2+ complex of the dipicolinoyl dipyrrolyl ketone was successfully analyzed by X-ray diffraction, which revealed an interesting tetranuclear Zn 2+ coordination structure. These results provide further insights into the design of highly sensitive Zn 2+ probes by introducing pyridyl moieties into dipyrrin platforms.

With the purpose to develop efficient dye-sensitized solar cells (DSSCs), a series of push-pull porphyrin dyes have been designed and optimized by introducing additional electron-donating diphenylamino and electron-withdrawing benzothiadiazole moieties. Electrochemical, photophysical and photovoltaic investigations indicate that the introduction of additional donors and acceptors can effectively extend the absorption spectra, resulting in better sunlight harvesting. However, the HOMO levels of the dyes are elevated by the additional donors, resulting in decreased driving forces for dye regeneration and decreased cell efficiencies. Upon coadsorption with 5 mM chenodeoxycholic acid (CDCA), the cell efficiencies can be elevated from 1.37% - 5.01% to 1.70% - 6.97%. Furthermore, based on the subtle absorption characteristics of the porphyrin dyes, we delicately designed a cocktail co-sensitization strategy using the solutions containing two of the porphyrin dyes as well as CDCA. Finally, a high photovoltaic efficiency of 8.6% was successfully achieved at an optimized molar ratio of 10:1 for the two porphyrin dyes.

A bidipyrrin nickel complex was synthesized in a high yield by oxidatively coupling between the ligands in the corresponding 2:1 (L:M) type of dipyrrin nickel complex, and further demetallation afforded the free bidipyrrin ligand. Interestingly, when treating the bidipyrrin nickel complex or the free bidipyrrin with FeCl3 in CH2Cl2/MeOH, the symmetric di-α-methoxy bidipyrrin could be synthesized in a high yield, with two methoxy groups attached to the terminal pyrrolic α-positions. Moreover, the coordination of the unsubstituted and disubstituted bidipyrrins with Zn(OAc)2·2H2O afforded two similar M2L2 type of bidipyrrin helical complexes with different ligand conformations and different Zn⋯Zn distances of 5.353 and 3.357 A, respectively. The difference in the conformations may be related to the electrostatic repulsions between the methoxy substituents. These results indicate that the dyes based on helical bidipyrrin zinc complexes with tunable structures and photophysical properties may be developed simply by modulating the terminal α-substituents.