Biodegradable Ruthenium-Rhenium Complexes Containing Nanoamplifiers: Triggering ROS-Induced CO Release for Synergistic Cancer Treatment.

The constrained effectiveness of photodynamic therapy (PDT) has impeded its widespread use in clinical practice. Urgent efforts are needed to address the shortcomings faced in photodynamic therapy, such as photosensitizer toxicity, short half-life, and limited action range of reactive oxygen species (ROS). In this study, a biodegradable copolymer nanoamplifier is reported that contains ruthenium complex (Ru-complex) as photosensitizer (PS) and rhenium complex (Re-complex) as carbon monoxide (CO)-release molecule (CORM). The well-designed nanoamplifier brings PS and CORM into close spatial proximity, significantly promotes the utilization of light-stimulated reactive oxygen species (ROS), and cascaded amplifying CO release, thus enabling an enhanced synergistic effect of PDT and gas therapy for cancer treatment. Moreover, owing to its intrinsic photodegradable nature, the nanoamplifier exhibits good tumor accumulation and penetration ability, and excellent biocompatibility in vivo. These findings suggest that the biodegradable cascaded nanoamplifiers pave the way for a synergistic and clinically viable integration of photodynamic and gas therapy.

Intramolecular Photoinduced Energy and Electron Transfer Reactions in Phenanthroimidazole-Boron Dipyromethane Donor-Acceptor Dyads.

Donor-acceptor systems in which a donor phenanthroimidazole (PhI) is directly connected to a BODIPY acceptor (Dyad1) and separated by an ethynyl bridge between PhI and BODIPY (Dyad2) have been designed, synthesized, and characterized by various spectroscopic and electrochemical techniques. Optical absorption and 1H NMR characteristics of both dyads with those of constituent individuals suggest that there exists a minimum π-π interaction between phenanthroimidazole and BODIPY. Quenched emission of both the dyads was observed when excited either at phenthaoimidazole absorption maxima or at BODIPY absorption maxima in all three investigated solvents. The detailed spectral analysis provided evidence for an intramolecular photoinduced excitation energy transfer (PEnT) from the singlet excited state of phenanthroimidazole to BODIPY and photoinduced electron transfer (PET) from the ground state of phenanthroimidazole to BODIPY. Transient absorption studies suggest that charge-separated species (PhI•+ - BODIPY•-) are generated at a rate constant of (1.16 ± 0.01) × 108 s-1 for the dyads Dyad1 and (5.15 ± 0.03) × 108 s-1 and for Dyad2 whereas energy transfer rate constants were much higher and were on the order of (1.1 ± 0.02) × 1010 s-1 and (1.6 ± 0.02) × 1010 s-1 for Dyad1 and Dyad2, respectively, signifying their usefulness in light energy harvesting applications.

Phenothiazine functionalized fulleropyrrolidines: synthesis, charge transport and applications to organic solar cells.

A series of phenothiazine-C60/70 dyads containing fulleropyrrolidine tethered to C-3 position (C60-PTZ and C70-PTZ) or to the heteroatom N-position via either phenyl (C60-Ph-PTZ and C70-Ph-PTZ) or phenoxyethyl linkers (C60-PhOEt-PTZ and C70-PhOEt-PTZ) of the phenothiazine were synthesized and light-induced electron transfer events were explored. Optimized studies suggested that the highest molecular orbital (HOMO) resides on donor phenothiazine moiety while lowest molecular orbital (LUMO) on the acceptor fulleropyrrolidine moiety of the dyads. Optical and electrochemical properties suggested no electronic communication between the donor and acceptor moieties in the ground state. However, steady-state emission studies in solvents of varied polarity, involving selective excitation of C60/C70, disclosed that the emission intensity of C60/C70 was quenched in the dyads in the increasing order, C60/70-PTZ > C60/70-Ph-PTZ > C60/70-PhOEt-PTZ as a consequence of the donor-acceptor distance resulted due to spacer lengths. Also, the emission quenching is more pronounced in polar solvents such as DMF compared to a non-polar solvent, toluene. With the support of parallel electrochemical studies, the emission quenching is attributed to intramolecular photo-induced electron transfer occurring from PTZ to (C60/C70)* generating a radical ion pair, PTZ+⋅-C60-⋅/PTZ+⋅-C70-⋅. Finally, bulk heterojunction (BHJ) solar cells devices inverted fashion prepared by employing the dyads as acceptors, and PTB7 as donor, suggested that the devices prepared from C70 derivatives i.e., PTB7:C70-PTZ and PTB7:C70-PhOEt-PTZ exhibited better power conversion efficiency of 2.66% and 2.15%, respectively over C60 derivatives i.e., PTB7:C60-PTZ and PTB7:C60-PhOEt-PTZ with the efficiencies of 1.80 and 1.72%, respectively. AFM studies revealed that the poor performance of PTB7:C60-PTZ- and PTB7:C60-PhOEt-PTZ-based devices can be ascribed to the lower solubility of the dyads in 1,2-DCB solvent leading to rough morphology.

Photoinduced energy transfer in carbazole-BODIPY dyads.

A series of carbazole (CBZ)-boron dipyrromethene (BODIPY) based donor-acceptor dyads, CB1, CB2, and CB3, with CBZ as an energy donor, tethered together with spacers of varied sizes i.e., phenyl bridge, biphenyl bridge and diphenylethyne bridge, respectively, are reported. The newly synthesized dyads were characterized by various spectroscopic techniques. A comparison of the absorption and electrochemical data of the dyads with their reference compounds (i.e., 9-phenyl-9H-carbazole (C0) and N,N'-difluoroboryl-1,3,7,9-tetramethyl-5-phenyldipyrrin (B0)) revealed minimal ground-state interactions between the chromophores. Selective excitation of CBZ in the dyads at 290 nm resulted in the quenching of the CBZ emission followed by the appearance of BODIPY emission, revealing efficient energy transfer from singlet excited CBZ (1CBZ*) to BODIPY. The photoinduced energy transfer phenomenon was studied in three different solvents of varying polarity. The driving forces for energy transfer (ΔGEN) for all the dyads were found to be exothermic. The rate constants for energy transfer, kENT, measured by the femtosecond transient absorption technique in toluene were found to be in the range of 0.8-2.0 × 1010 s-1, depending on the type of spacer between the CBZ and BODIPY entities, and were in close agreement with the theoretically estimated rates according to the Förster energy transfer model. In contrast, selective excitation of BODIPY in these dyads at 485 nm resulted in small quenching of the BODIPY emission, suggesting a lack of major photochemical events originating from 1BODIPY*.

Excitation-dependent electron exchange energy and electron transfer dynamics in a series of covalently tethered N,N-bis(4'-tert-butylbiphenyl-4-yl)aniline - [C60] fullerene dyads via varying π-conjugated spacers.

Femtosecond time-resolved fluorescence and transient absorption studies are reported for three newly synthesized covalently linked N,N-bis(4'-tert-butylbiphenyl-4-yl)aniline (BBA) and pyrrolidinofullerenes (C60)-based donor-π conjugated bridge-acceptor dyads (D-B-A) as functions of the bridge length (7.1, 9.5 and 11.2 Å for Dyad-1, Dyad-2 and Dyad-3), dielectric constants of the medium and pump wavelengths. In polar solvent, ultrafast fluorescence quenching (kEET ≥ 2 × 1012 s-1) of the BBA moiety upon excitation of the BBA moiety (320 nm) is observed in the dyads and is assigned to a mechanism involving electron exchange energy transfer (EET) from 1BBA* to C60 followed by electron transfer from BBA to 1C60*. Cohesive rise and decay dynamics of conjugated BBA˙+-C60˙- anion pairs confirm the involvement of a distance independent adiabatic charge-separation (CS) process (kCS ≥ 2.2 × 1011 s-1) with near unity quantum efficiency (φCS ≥ 99.7%) and a distance-dependent non-adiabatic charge-recombination (CR) process [kCR ∼ (1010-108) s-1]. In contrast, excitation of the C60 moiety (λex = 430 to 700 nm) illustrates photoinduced electron transfer from BBA to 1C60*, involving non-adiabatic (diabatic) and distance-dependent CS (kCS in the range of 0.59-1.78 × 1011 s-1) with 98.86-99.6% (Dyad-3-Dyad-1) quantum efficiency and a CR process with kCR values [kCR ∼ (1010-108) s-1] up to three orders greater than kCS of the respective dyads. Both the processes, CS and CR, upon C60 excitation and the CR process upon BBA excitation show distance dependent rate constants with exponential factor ß ≤ 0.5 Å-1, and electron transfer is concluded to occur through a covalently linked conjugated π bridge. Global and target analysis of fsTA data reveal the occurrence of two closely lying CS states, thermally hot (CShot) and thermally relaxed (CSeq) states, and two CR processes with two orders of different rate constants. Careful analysis of the kinetic and thermodynamic data allowed us to estimate the total reorganization energy and electronic coupling matrix (V), which decrease exponentially with distance. These novel features of the distance independent adiabatic CS process and the distance-dependent diabatic CR process upon donor excitation are due to extending the π-conjugation between BBA and C60. The demonstrated results may provide a benchmark in the design of light-harvesting molecular devices where ultrafast CS processes and long-lived CS states are essential requirements.

Hypochlorite-Mediated Modulation of Photoinduced Electron Transfer in a Phenothiazine-Boron dipyrromethene Electron Donor-Acceptor Dyad: A Highly Water Soluble "Turn-On" Fluorescent Probe for Hypochlorite.

A highly water-soluble phenothiazine (PTZ)-boron dipyrromethene (BODIPY)-based electron donor-acceptor dyad (WS-Probe), which contains BODIPY as the signaling antennae and PTZ as the OCl- reactive group, was designed and used as a fluorescent chemosensor for the detection of OCl- . Upon addition of incremental amounts of NaOCl, the quenched fluorescence of WS-Probe was enhanced drastically, which indicated the inhibition of reductive photoinduced electron transfer (PET) from PTZ to 1 BODIPY*; the detection limit was calculated to be 26.7 nm. Selectivity studies with various reactive oxygen species, cations, and anions revealed that WS-Probe was able to detect OCl- selectively. Steady-state fluorescence studies performed at varied pH suggested that WS-Probe can detect NaOCl and exhibits maximum fluorescence in the pH range of 7 to 8, similar to physiological conditions. ESI-MS analysis and 1 H NMR spectroscopy titrations showed the formation of sulfoxide as the major oxidized product upon addition of hypochlorite. More interestingly, when WS-Probe was treated with real water samples, the fluorescence response was clearly visible with tap water and disinfectant, which indicated the presence of OCl- in these samples. The in vitro cell viability assay performed with human embryonic kidney 293 (HEK 293) cells suggested that WS-probe is non-toxic up to 10 µm and implicates the use of the probe for biological applications.