9-Borafluoren-9-yl and diphenylboron tetracoordinate complexes of F- and Cl-substituted 8-quinolinolato ligands: synthesis, molecular and electronic structures, fluorescence and application in OLED devices.

Six new four-coordinate tetrahedral boron complexes, containing 9-borafluoren-9-yl and diphenylboron cores attached to orthogonal fluorine- and chlorine-substituted 8-quinolinolato ligand chromophores, have been synthesised, characterised, and applied as emitters in organic light-emitting diodes (OLEDs). An extensive steady-state and time-resolved photophysical study, in solution and in the solid state, resulted in the first-time report of delayed fluorescence (DF) in solid films of 8-quinolinolato boron complexes. The DF intensity dependence on excitation dose suggests that this emission originates from triplet-triplet annihilation (TTA). Density functional theory (DFT) and time-dependent density functional theory (TDDFT) studies give insight into the ground and excited state geometries, electronic structures, absorption energies, and singlet-triplet gaps in these new organoboron luminophores. Finally, given their highly luminescent behaviour, organic light-emitting diode (OLED) devices were produced using the synthesised organoboron compounds as emissive fluorescent dopants. The best OLED displays green-blue (λmaxEL = 489 nm) electroluminescence with an external quantum efficiency (EQE) of 3.3% and a maximum luminance of 6300 cd m-2.

Spectroscopic Analysis of Parathyroid and Thyroid Tissues by Ground-State diffuse Reflectance and Laser Induced Luminescence: a Preliminary Report.

Intraoperative discrimination of thyroid and parathyroid tissues is fundamental in thyroid surgery. Recent fluorescence studies have shown stronger NIR emission in parathyroid tissue than in thyroid tissue, presenting a potential avenue for the development of a tool for surgical assistance. However, the fluorophore responsible for this emission has not yet been identified. In this work, spectroscopic analysis was performed to ascertain the origin of the emission peaks in parathyroid tissue. Ground-state diffuse reflectance (GSDR) absorption spectroscopy and laser-induced luminescence (LIL) emission spectroscopy were performed in parathyroid, thyroid, and fatty tissue samples and the resulting spectra were compared with the peaks of known fluorophores to identify the origin of each peak. The spectra of the different tissue types were also compared in order to evaluate the wavelength which presents the highest parathyroid emission relative to the emission of the surrounding tissues, representing the ideal wavelength for parathyroid detection. An emission peak in these conditions was observed for both thyroid and parathyroid tissue at 711 nm, with a higher intensity in parathyroid sample, making it suitable for detection applications. These results show a potential avenue for the development of a system allowing parathyroid detection in a surgical setting.

Versatility of Amide-Functionalized Co(II) and Ni(II) Coordination Polymers: From Thermochromic-Triggered Structural Transformations to Supercapacitors and Electrocatalysts for Water Splitting.

The new 2D coordination polymers (CPs) [M(L)2(H2O)2]n [M = CoII (1) and NiII (2); L = 4-(pyridin-3-ylcarbamoyl)benzoate] were synthesized from pyridyl amide-functionalized benzoic acid (HL). They were characterized by elemental, Fourier transform infrared, thermogravimetric, powder X-ray diffraction (PXRD), and single-crystal X-ray diffraction (XRD) structural analyses. Single-crystal XRD analysis revealed the presence of a 2D polymeric architecture, and topological analyses disclose a 2,4-connected binodal net. A thermochromic effect leads to the production of two new CPs, 1' and 2', by heating at ca. 220 °C, accompanied by a color change from orange to purple in the case of 1 and from blue to green in the case of 2. The transformation of 1 to 1' takes place through an intermediate (1a) with a different twist of the L- ligand, leading to the formation of a 1D polymeric architecture, as proven by single-crystal XRD analysis. The addition of water or keeping 1' or 2' in air for several days leads to regeneration of 1 or 2, respectively. The thermochromic-triggered structural transformations of 1 and 2 were further substantiated by PXRD and UV-vis ground-state diffuse-reflectance absorption studies. The supercapacitance ability of the CPs 1 and 2 and a Ni-Co composite (made from mixing the CPs 1 and 2) was investigated by electroanalytical techniques, such as cyclic voltammetry and electrochemical impedance spectroscopy. The CP 2 exhibits the highest specific capacity of 273.8 C g-1 at an applied current density of 1.5 A g-1. These newly developed CPs further act as electrocatalysts for the water-splitting reaction.

Facile functionalization of cotton with nanostructured silver/titania for visible-light plasmonic photocatalysis.

In the present work, a simple, reliable and cost-effective approach to functionalize cotton fabrics with Ag-TiO2 nanoparticles strongly bound to the fibres and with visible-light-responsive photo-activity is presented. The hybrid cotton-Ag-TiO2 fabrics were characterized by Raman, AFM, FE-SEM, TGA, XPS GSDR, and LIL to confirm the generation of metallic Ag nanoparticles and crystalline TiO2 and investigate how the concentration of Ag and TiO2 precursors affected the morphology and the luminescence properties of the nanostructured layer grafted on the cotton fibres. The photocatalytic activity of the cotton-Ag-TiO2 hybrid systems was evaluated by the discoloration of Remazol Brilliant Blue R in water under a xenon lamp irradiation (sunlight simulator) equipped with selective filters. The extended photocatalytic activity to the visible is here explained by a synergistic effect of both the excitation of the Ag NPs plasmon resonance by visible light and a delayed electron-hole recombination rate caused by Ag NPs, as it can be observed by UV absorption.

Surface photochemistry: 3,3'-dialkylthia and selenocarbocyanine dyes adsorbed onto microcrystalline cellulose.

In this work, thia and selenocarbocyanines with n-alkyl chains of different length, namely with methyl, ethyl, propyl, hexyl and decyl substituents, were studied in homogeneous and heterogeneous media for comparison purposes. For both carbocyanine dyes adsorbed onto microcrystalline cellulose, a remarkable increase in the fluorescence quantum yields and lifetimes were detected, when compared with solution. Contrary to the solution behaviour, where the increase in the n-alkyl chains length increases to a certain extent the fluorescence emission Φ(F) and τ(F), on powdered solid samples a decrease of Φ(F) and τ(F) was observed. The use of an integrating sphere enabled us to obtain absolute Φ(F)'s for all the powdered samples. The main difference for liquid homogeneous samples is that the increase of the alkyl chain strongly decreases the Φ(F) values, both for thiacarbocyanines and selenocarbocyanines. A lifetime distribution analysis for the fluorescence of these dyes adsorbed onto microcrystalline cellulose, evidenced location on the ordered and crystalline part of the substrate, as well as on the more disordered region where the lifetime is smaller. The increase of the n-alkyl chains length decreases the photoisomer emission for the dyes adsorbed onto microcrystalline cellulose, as detected for high fluences of the laser excitation, for most samples.

Surface photochemistry of pesticides containing 4-chlorophenoxyl chromophore.

The surface photochemistry of pesticides containing 4-chlorophenoxyl chromophore was accessed on the model surfaces cellulose and silica, using diffuse reflectance and chromatographic techniques. 4-Chloroanisole was chosen as the model compound and its phototransformation was followed under lamp (254 nm) and sunlight irradiation. The photodegradation rates are faster on cellulose than on silica. The main photodegradation products on cellulose are anisole and dimerization compounds while on silica the formation of 4-hydroxyanisole and dimerization are the main reaction pathways. Transient absorption studies showed the formation of the 4-methoxyphenylperoxyl radical only on cellulose and in the presence of oxygen. The homolytic cleavage of the C-Cl bond, and consequent formation of a triplet radical pair, is the main primary reaction step on both surfaces. The radical pair then diffuses apart or undergoes electron transfer to form phenyl radicals and phenyl cations, respectively. These two reaction intermediates account for reduction, addition, and formation of bonded residues, the main reactions observed on the studied surfaces and also expected to prevail under natural conditions.

Surface photochemistry: organic molecules within nanocavities of calixarenes.

In order to gain more information regarding photochemical processes in heterogeneous environments (opaque or powdered samples) laser induced time resolved luminescence and diffuse reflectance transient absorption spectroscopies were used for the study of benzophenone (and other neutral organic molecules) as guests and p-tert-butylcalix[n]arenes with n = 4, 6 and 8 (H(n)CLX[n]) and partially or totally O-propylated p-tert-butylcalix[4]arenes (H(n)Pr(m)CLX[4], n = 2, 1 and 0; m = 2, 3 and 4, respectively) were used as hosts. One of the main conclusions was that the solid support can deeply affect or even control the photochemistry of an adsorbed probe. A simple new methodology for lifetime distribution analysis of the decay of the probes included into calixarenes and other nanocavities was applied with success for decay data obtained with the use of intensified charge couple devices, i.e. intensified charge couple devices, ICCDs. Diffuse reflectance laser flash photolysis and gas chromatography - mass spectrometry techniques also provided complementary information, the former about transient species and the latter regarding the final products formed after light absorption.

Luminescence lifetime distributions analysis in heterogeneous systems by the use of Excel's Solver.

A detailed study of the luminescence decay curves of pyrene included within p-tert-butylcalix[4]arene cavities and benzophenone into silicalite channels is reported. A new methodology for a lifetime distribution analysis of the decay curve of probes onto heterogeneous surfaces is presented, which allows for asymmetric distributions and uses Voigt profiles (Gaussian and Lorentzian mixture) instead of pure Gaussian or Lorentzian distributions. Our approach uses a very simple and widely available tool for fitting, the Microsoft Excel Solver. In the case of the pyrene/tert-butylcalix[4]arene sample, the room temperature luminescence detected in the microsecond time scale was not only the phosphorescence of pyrene but also monomer delayed fluorescence, crystal phosphorescence, and excimer delayed fluorescence. In the benzophenone/silicalite case, three emissive forms of benzophenone could be assigned, one of benzophenone included into the silicalite circular zigzag channels, another for emplacement into the elliptical straight channels and finally when benzophenone is placed at the crossing points of those silicalite channels, where smaller spatial restrictions for benzophenone exist.

Surface photochemistry of pesticides: an approach using diffuse reflectance and chromatography techniques.

The photochemistry of pesticides triadimenol and triadimefon was studied on cellulose and beta-cyclodextrin (beta-CD) in controlled and natural conditions, using diffuse reflectance techniques and chromatographic analysis. The photochemistry of triadimenol occurs from the chlorophenoxyl moiety, while the photodegradation of triadimefon also involves the carbonyl group. The formation of 4-chlorophenoxyl radical is one of the major reaction pathways for both pesticides and leads to 4-chlorophenol. Triadimenol also undergoes photooxidation and dechlorination, leading to triadimefon and dechlorinated triadimenol, respectively. The other main reaction process of triadimefon involves alpha-cleavage from the carbonyl group, leading to decarbonylated compounds. Triadimenol undergoes photodegradation at 254 nm but was found to be stable at 313 nm, while triadimefon degradates in both conditions. Both pesticides undergo photochemical decomposition under solar radiation, being the initial degradation of rate per unit area of triadimefon 1 order of magnitude higher than the observed for triadimenol in both supports. The degradation rates of the pesticides were somewhat lower in beta-CD than on cellulose. Photoproduct distribution of triadimenol and triadimefon is similar for the different irradiation conditions, indicating an intramolecular energy transfer from the chlorophenoxyl moiety to the carbonyl group in the latter pesticide.

Structure and photoluminescence of a benzil nanocolumn in a C-methylcalix[4]resorcinarene-based framework.

A new framework based on C-methylcalix[4]resorcinarene and the flexible nonconjugated spacer 1,4-bis(imidazol-1yl-methyl)benzene encloses a large one-dimensional channel, containing benzil nanocolumns. Unlike in a previously reported series of benzil-containing supramolecular solids with conjugated linker molecules, benzil luminescence is observed, but the lifetime of 580 ns at 77 K is considerably shorter than the 145 micros reported for neat benzil at room temperature.

A diffuse reflectance comparative study of benzil inclusion within microcrystalline cellulose and beta-cyclodextrin.

Diffuse reflectance and laser-induced techniques were used to study photochemical and photophysical processes of benzil adsorbed on two solid powdered supports, microcrystalline cellulose and [small beta]-cyclodextrin. In both substrates, a distribution of ground-state benzil conformers exists, largely dominated by skew conformations where the carbonyl groups are twisted one to the other. Room temperature phosphorescence was observed in air-equilibrated samples in both cases. The decay times vary greatly and the largest lifetime was obtained for benzil/[small beta]-cyclodextrin, showing that this host's cavity accommodates benzil well, enhancing its room temperature phosphorescence. Triplet-triplet absorption of benzil entrapped in cellulose was detected and benzil ketyl radical formation also occurred. With benzil included into [small beta]-cyclodextrin, and following laser excitation, benzoyl radicals were detected on the millisecond timescale. Product analysis and identification of laser-irradiated benzil samples in the two hosts clearly showed that the main degradation photoproducts were benzoic acid and benzaldehyde. The main differences were a larger benzoic acid/benzaldehyde ratio in the case of cellulose and the formation of benzyl alcohol in this support.

Luminescence quantum yield determination for molecules adsorbed onto solid powdered particles.

A new methodology for the determination of the fluorescence quantum yield of dyes adsorbed onto microcrystalline cellulose is presented and applied to rhodamine 101, cresyl violet and auramine O. It is based on a previously reported method by Ruetten and Thomas (J. Phys. Chem., 1998, 102, 598-606), which is not applicable to the dyes used in the present study. It uses ground-state diffuse reflectance spectra obtained with and without filters, which prevents the luminescence of the dye from reaching the integrating sphere and the photodetector. New equations are presented here, correcting for the fluorescence emission of the dye, which depends on the detector sensitivity. Cut-on filters, which have a transmittance close to unity in the absorption region, and close to zero in the emission region, of the dye are used to obtain corrected reflectance spectra. The influence of the substrate was also taken into account. This methodology may be applied to other probes and surfaces or emissions of a different nature (i.e., phosphorescence or delayed fluorescence), and constitutes a very simple and general procedure to solve the important problem of luminescence quantum yield determination of probes adsorbed onto solid powdered surfaces.

Novel laser-induced luminescence resulting from benzophenone/O-propylated p-tert-butylcalix[4]arene complexes. A diffuse reflectance study.

Laser-induced room temperature luminescence of air-equilibrated benzophenone/O-propylated p-tert-butylcalix[4]arene solid powdered samples revealed the existence of a novel emission, in contrast with benzophenone/p-tert-butylcalix[4]arene complexes, where only benzophenone emits. This novel emission was identified as phosphorescence of 1-phenyl-1,2-propanedione, which is formed as the result of an hydrogen atom abstraction reaction of the triplet excited benzophenone from the propoxy substituents of the calixarene. Room temperature phosphorescence was obtained in air-equilibrated samples in all propylated hosts. The decay times of the benzophenone emission vary greatly with the degree of propylation, the shortest lifetimes being obtained in the tri- and tetrapropylated calixarenes. Triplet-triplet absorption of benzophenone was detected in all cases, and is the predominant absorption in the p-tert-butylcalix[4]arene case. where an endo-calix complex is formed. Benzophenone ketyl radical formation occurs with the O-propylated p-tert-butylcalix[4]arenes hosts, suggesting a different type of host/guest molecular arrangement. Diffuse reflectance laser flash photolysis and gas chromatography-mass spectrometry techniques provided complementary information, the former about transient species and the latter regarding the final products formed after light absorption. Product analysis and identification clearly show that the two main degradation photoproducts following laser excitation in the propylated substrates are 1-phenyl-1,2-propanedione and 2-hydroxybenzophenone, although several other minor photodegradation products were identified. A detailed mechanistic analysis is proposed. While the solution photochemistry of benzophenone is dominated by the hydrogen abstraction reaction from suitable hydrogen donors, in these solid powdered samples, the alpha-cleavage reaction also plays an important role. This finding occurs even with one single laser pulse which lasts only a few nanoseconds, and is apparently related to the fact that scattered radiation exists, due to multiple internal reflections possibly trapping light within non-absorbing microcrystals in the sample, and is detected until at least 20 micros after the laser pulse. This could explain how photoproducts thus formed could also be excited with only one laser pulse.

Photochemistry of 4-chlorophenol on cellulose and silica.

The photochemistry of 4-chlorophenol (4-CP) was studied on silica and cellulose, using time-resolved diffuse reflectance techniques and product degradation analysis. The results have shown that the photochemistry of 4-CP depends on the support, on the concentration, and also on the sample preparation method. Transient absorption and photoproduct results can be understood by assuming the formation of the carbene 4-oxocyclohexa-2,5-dienylidene in both supports. On cellulose, at concentrations lower than 10 micromol g(-1), the carbene leads to the unsubstituted phenoxyl radical, and phenol is the main degradation product. At higher concentrations a new transient resulting from phenoxyl radicals coupling was also observed, and dihydroxybiphenyls are also formed. The reaction of the carbene with ground-state 4-CP was also detected through the formation of 5-chloro-2,4'-dihydroxybiphenyl. 4-Chlorophenoxyl radical and degradations products resulting from its coupling were also detected. Oxygen has little effect on the photochemistry of 4-CP on cellulose. On silica the transient benzoquinone O-oxide was formed in the presence of oxygen. Benzoquinone and hydroquinone are the main degradation products. In well-dried samples the formation of hydroquinone is reduced. At higher concentrations the same products as detected on cellulose were observed. 4-CP undergoes slow photochemical decomposition under solar radiation in both supports. The same main degradation products were observed in these conditions.