Luminescent 2-phenylbenzothiazole cyclometalated PtII and IrIII complexes with chelating P

Two series of cyclometalated PtII and IrIII complexes with general formulas [Pt(pbt){PPh2(R)-κP,O}] (2a-2c) and [Ir(pbt)2{PPh2(R)-κP,O}] (3a-3c), where Hpbt is 2-phenylbenzothiazol and PPh2(R) is a diphenylphosphino donor functionalized deprotonated acid (R = o-C6H4CO2a, o-C6H4SO3b, CH2CH2CO2c) are presented. The structures of 1, 2a-2c, 3a and 3b were confirmed by single X-ray diffraction analyses, and the intermolecular interactions in 2a were studied using Hirshfeld surface analysis and non-covalent interaction (NCI) methods on its X-ray structure. Their photophysical properties were investigated by absorption and emission analyses [CH2Cl2, solid (298, 77 K) and doped polystyrene (PS) films], supported by TD-DFT calculations on 1, 2a-2c and 3a. The PtII complexes exhibit bright phosphorescence in the region 525-542 nm, ascribed to a mixed 3IL/3MLCT excited state with a predominant 3IL contribution. The IrIII derivatives (3a-3c) show orange photoluminescence (535-584 nm, 298 K), blue shifted at 77 K (527-560 nm), originated from the admixture of 3IL/3MLCT/3LLCT excited states. Interestingly, the photoluminescence quantum yields of the Pt complexes 2a-2c (ϕ = 46.5-66.5%) in PS films are remarkably higher than those of the corresponding iridium complexes (ϕ = 17.3-32%) and the precursor 1 (ϕ = 17%). The calculated 3MC-3IL/3MLCT energy gap for 2a and 3a accounts for the higher quantum yield of the Pt in relation to the Ir complex.

Investigation on Optical and Biological Properties of 2-(4-Dimethylaminophenyl)benzothiazole Based Cycloplatinated Complexes.

The optical and biological properties of 2-(4-dimethylaminophenyl)benzothiazole cycloplatinated complexes featuring bioactive ligands ([{Pt(Me2 N-pbt)(C6 F5 )}L] [L=Me2 N-pbtH 1, p-dpbH (4-(diphenylphosphino)benzoic acid) 2, o-dpbH (2-(diphenylphosphino)benzoic acid) 3), [Pt(Me2 N-pbt)(o-dpb)] 4, [{Pt(Me2 N-pbt)(C6 F5 )}2 (µ-PRn P)] [PR4 P=O(CH2 CH2 OC(O)C6 H4 PPh2 )2 5, PR12 P=O{(CH2 CH2 O)3 C(O)C6 H4 PPh2 }2 6] are presented. Complexes 1-6 display 1 ILCT and metal-perturbed 3 ILCT dual emissions. The ratio between both bands is excitation dependent, accomplishing warm-white emissions for 2, 5 and 6. The phosphorescent emission is lost in aerated solutions owing to photoinduced electron transfer to 3 O2 and the formation of 1 O2 , as confirmed in complexes 2 and 4. They also exhibit photoinduced phosphorescence enhancement in non-degassed DMSO due to local oxidation of DMSO by sensitized 1 O2 , which causes a local degassing. Me2 N-pbtH and the complexes specifically accumulate in the Golgi apparatus, although only 2, 3 and 6 were active against A549 and HeLa cancer cell lines, 6 being highly selective in respect to nontumoral cells. The potential photodynamic property of these complexes was demonstrated with complex 4.

Perfil epidemiológico de cirurgias em serviço de urgência e emergência / Epidemiological profile of surgery in emergency service

RESUMO: Introdução: A encefalite viral é uma condição com altas taxas de morbimortalidade, e um melhor entendimento de sua epidemiologia pode colaborar para a construção de estratégias de prevenção e controle. Diante disso, este estudo se propôs a traçar um perfil epidemiológico para a encefalite viral no Brasil no ano de 2018 a partir de dados de internações hospitalares no Sistema Único de Saúde (SUS). Métodos: Estudo ecológico de análise espacial. Os dados estudados foram relativos às internações hospitalares por encefalite viral no SUS em 2018, estratificadas por unidade da federação (UF), sexo e faixa etária. A distribuição geográfica foi abordada exploratoriamente, já as variáveis sexo e faixa etária foram abordadas analiticamente. Resultados: Foram registradas 2075 internações, com taxa de 0,99/105 habitantes. As taxas para cada UF foram representadas a partir de um mapa colorimétrico, enquanto as taxas para cada sexo e faixa etária foram representadas em uma tabela comparativa univariada. Discussão: Observou-se ampla variação numérica das taxas de internação dentre as UF, sendo Pernambuco o estado com maior incidência (4,13/105 habitantes) e Paraíba o estado com menor (0,29/105 habitantes). Foi constatada associação significativa com o risco de internação hospitalar por encefalite viral para o sexo masculino e para as faixas etárias de 1 a 4 anos (RR: 3,28) e menores de 1 ano (RR: 6,02). Conclusão: UF, gênero e faixa etária foram determinantes importantes da taxa de internação hospitalar por encefalite viral. Todavia, carecem de estudos atuais no Brasil e no mundo para a melhor caracterização da epidemiologia da encefalite viral. (AU)

ABSTRACT: Introduction: Viral encephalitis is a condition with high morbidity and mortality rates, and a better understanding of its epidemiology may contribute to the construction of prevention and control strategies. For this reason, this study aimed to draw an epidemiological profile for viral encephalitis in Brazil in 2018 from data on hospitalizations in the Unified Health System (SUS). Methods: Ecological study of spatial analysis. The data studied were hospitalizations for viral encephalitis in SUS in 2018, stratified by federation unit (FU), gender, and age group. The geographical distribution was approached in an exploratory way, whereas gender and age variables were analytically addressed. Results: There were 2075 hospitalizations, with a rate of 0.99/105 inhabitants. The rates for each FU were represented in a colorimetric map, whereas the rates for each sex and age group were exemplified in a univariate comparative table. Discussion: There was a wide numerical variation in hospitalization rates among the FUs, with Pernambuco being the state with the highest incidence (4.13/105 inhabitants) and Paraíba with the lowest (0.29/105 inhabitants). A significant association was found with the risk of hospitalization for viral encephalitis for males and the ages from 1 to 4 years (RR: 3.28) and under one year (RR: 6.02). Conclusion: FU, gender, and age group were important determinants of the hospitalization rate due to viral encephalitis. However, current studies are needed in Brazil and worldwide to better characterize the epidemiology of viral encephalitis. (AU)

Design of Luminescent, Heteroleptic, Cyclometalated PtII and PtIV Complexes: Photophysics and Effects of the Cyclometalated Ligands.

Neutral pentafluorophenyl benzoquinolinyl PtII [Pt(bzq)(HC^N-κN)(C6 F5 )] (1 a-g) complexes, bearing nonmetalated N-heterocyclic HC^N ligands [HC^N=2,5-diphenyl-1,3,4-oxadiazole (Hoxd) a, 2-(2,4-difluorophenyl)pyridine (dfppy) b, 2-phenylbenzo[d]thiazole (pbt) c, 2-(4-bromophenyl)benzo[d]thiazole (Br-pbt) d, 2-phenylquinoline (pq) e, 2-thienylpyridine (thpy) f, 1-(2-pyridyl)pyrene (pypy) g], and heteroleptic bis(cyclometalated) PtIV fac-[Pt(bzq)(C^N)(C6 F5 )Cl] (2 b-g, bzq: benzo[h]quinolinyl) derivatives, generated by oxidation of 1 b-g with PhICl2 , are reported. The oxidation reaction of 1 a evolved with formation of the bimetallic PtIV complex syn-[Pt(bzq)(C6 F5 )Cl(µ-OH)]2 3. The crystal structures of 1 a,d,f, 2 b,d,e and 3 were corroborated by X-ray crystallography. A comparative study of the absorption and photoluminescence properties of the two series of complexes PtII (1) and PtIV (2), supported by time-dependent DFT calculations (TD-DFT), is presented. The low-lying transitions (absorption and emission) of PtII complexes 1 a-e [solution and polystyrene (PS) films] were assigned to the IL/MLCT mixture located on the cyclometalated Pt(bzq) unit, with minor IL'/ML'CT/LL'CT contributions involving the non-metalated ligand. Complex 1 g, bearing the more delocalized pyridyl pyrene (Hpypy) as an ancillary ligand, shows dual 1 ππ* and 3 ππ* (Hpypy) emission in fluid CH2 Cl2 and dual 3 IL/3 MLCT [Pt(bzq)] and [3 ππ*, Hpypy] phosphorescence at 77 K. Upon oxidation, PtIV complexes 2 b-f display (solution, PS) ligand-based phosphorescence that arises from the bzq in 2 b (3 LC) or from the second C^N ligand in 2 c-f (3 L'C) with some 3 LL'CT in 2 f. Despite metalation of the pyrenyl group, 2 g exhibits dual emission 1 ππ*/3 ππ* located on the pypy chromophore.

Luminescent Cycloplatinated Complexes with Biologically Relevant Phosphine Ligands: Optical and Cytotoxic Properties.

Two series of neutral luminescent pentafluorophenyl cycloplatinated(II) complexes [Pt(C^N)(C6F5)L] [C^N = C-deprotonated 2-phenylpyridine (ppy; a), 2-(2,4-difluorophenylpyridine (dfppy; b)] incorporating dimethyl sulfoxide [L = DMSO for 1 (1a reported by us in ref (14) )] or biocompatible phosphine [L = PPh2C6H4COOH (dpbH; 2), PPh2C6H4CONHCH2COOMe (dpbGlyOMe; 3), P(C6H4SO3Na)3 (TPPTS; 4)] ligands have been prepared and characterized and their optical properties studied. Their cytotoxic activities against tumor A549 (lung carcinoma), HeLa (cervix carcinoma), and nontumor NL-20 (lung epithelium) cell lines, as well as the ability to interact with DNA (plasmid pBR322), were evaluated. Complexes 2 exhibit higher cytotoxicity (IC50 3.89-20.29 µM) than compounds 1 (9.03-20.50 µM), whereas the activities of complexes 3 and 4 are negligible. All cytotoxic complexes show low selective toxicities toward cancer cells. Interestingly, except 1a, these complexes do not show evidence of DNA intercalation. Along the same lines, fluorescence costaining with Hoechst (2,5'-bi-1 H-benzimidazole, 2'-(4-ethoxyphenyl)-5-(4-methyl-1-piperazinyl), a nuclear DNA stain) reveals that all complexes easily internalize, being mainly localized in the cytoplasm. In order to deepen the mechanism of biological action, the effect of the most cytotoxic complex 2b toward the dynamics of tubulin was explored. This complex displays tubulin depolymerization activity, exhibiting more potent inhibition of microtubule formation in A549 than in HeLa cells, in accordance with its higher antiproliferative activity (IC50 6.98 vs 12.45 µM), placing this complex as a potential antitubulin agent.

Benzothiazole-Based Cycloplatinated Chromophores: Synthetic, Optical, and Biological Studies.

Cycloplatinated complexes based on 2-(4-substituted)benzothiazole ligands of type [Pt(R-PBT-κC,N)Cl(L)] (PBT=2-phenylbenzothiazole; R=Br (1), Me2 N (2); L=dimethyl sulfoxide (DMSO; a), 1,3,5- triaza-7-phosphaadamantane (PTA; b), triphenylphosphine 3,3',3''-trisulfonate (TPPTS; c)) and [Pt(Br-PBT-κC)Cl(PTA)2 ] (3) are presented. On the basis of the photophysical data and time-dependent (TD)-DFT calculations (1 a and 2 a), the low-lying transitions (absorption and emission) were associated with ligand-center (LC) charge transfer, with minor metal-to-ligand charge transfer (MLCT), and intraligand charge transfer (ILCT) [Me2 N-PBT→PBT] excited states, respectively. Simultaneous fluorescence/phosphorescence bands were found in fluid solutions (and also in the solid state for 2 a), which become dominated by triplet emission bands in rigid media at 77 K. The effect of the concentration on emissive behavior of 2 a, b indicated the occurrence of aggregation-induced luminescence properties related to the occurrence of metal-metal and π⋅⋅⋅π interactions, which are more enhanced in 2 a because of the less bulky DMSO ligand. The behavior of 2 a toward para-toluenesulfonic acid (PTSA) in aerated acetonitrile and to hydrogen chloride gas in the solid state has been evaluated, thus showing a clear reversible change between the 1 ILCT and 3 LC/3 MLCT states due to protonation of the NMe2 group (theoretical calculations on 2 a-H+ ). Solid 2 a undergoes a surprising oxidation of the PtII center to PtIV with concomitant deoxygenation of DMSO, under prolonged reaction with hydrogen chloride gas to afford the PtIV /dimethyl sulfide complex (mer-[Pt(Me2 N-PBT-κC,N)Cl3 (SMe2 )]; mer-4), which evolves in solution to fac-4, as confirmed by X-ray studies. Cytotoxic activity studies on A549 and HeLa cell lines indicated cytotoxic activity of 1 b and 2 a, b. In addition, fluorescent cell microscopy revealed cytoplasmic staining, more visible in perinuclear areas. Inhibition of tubulin polymerization by 1 b in both cells is presented as a preliminary mechanism of its cytotoxic action.

Facile Approaches to Phosphorescent Bis(cyclometalated) Pentafluorophenyl PtIV Complexes: Photophysics and Computational Studies.

A convenient and general strategy for the synthesis of stable bis(cyclometalated) pentafluorophenyl PtIV complexes fac-[Pt(C^N)2 (C6 F5 )Cl] (3 a-f) and mer-[Pt(C^N)2 (C6 F5 )(CN)] (4 c,d) has been developed. Complexes 3 were selectively generated by low-temperature oxidation of the cyclometalated PtII complexes [Pt(C^N)(HC^N)(C6 F5 )] 2 [prepared from cis-[Pt(C6 F5 )2 (HC^N)2 ] (1) intermediates] with PhICl2 and subsequent metalation of the pendant HC^N ligand. Complexes 3 a,b were also alternatively generated by irradiation (Hg lamp, 400 W) of complexes 2 a,b, respectively, in CH2 Cl2 . This latter reaction proceeds via the hydride PtIV species cis-[Pt(C^N)2 (C6 F5 )H], detected as the only intermediate species. The molecular structures of 1 a,d, 2 a, and 3 a,b,d,e were confirmed by X-ray diffraction. The substitution of Cl- by CN- in fac-[Pt(C^N)2 (C6 F5 )Cl] [C^N=2-phenylbenzothiazole (3 c), 2-(4-bromophenyl)benzothiazole (3 d)] evolved with isomerization to give rise to the isomers (OC-6-42)-[Pt(C^N)2 (C6 F5 )(CN)] (4 c, 4 d) having a mer disposition of the cyclometalated and C6 F5 groups (X-ray, 4 c). All the complexes are luminescent and their electronic spectra have been compared and interpreted with the aid of time-dependent DFT calculations.

Phosphorescent platinum(ii) alkynyls end-capped with benzothiazole units.

Symmetric trans-bis(alkynyl)bis(phosphine) PtII complexes based on the 2-phenylbenzothiazole (pbt) unit [trans-Pt(C[triple bond, length as m-dash]C-pbt)2L2] [L = PPh31, PEt32, 1,3,5-triaza-7-phosphaadamantane (PTA) 3] and the mixed alkynyl-cyanide anionic complex (NBu4)2[trans-Pt(C[triple bond, length as m-dash]C-pbt)2(CN)2] (4) were synthesized. The complexes have been fully characterized including X-ray crystallography for 2 and 4. All complexes display long-lived emission with moderate quantum yields (ϕ 6.8-22.6%) in doped PMMA films at 298 K and complex 4 is also emissive in DMSO fluid and in rigid media (solid, glass at 77 K). Complex 4 displays a negative solvatochromic behavior. Absorption and emission energies have been analyzed by means of linear solvation energy based on Kamlet-Taft solvatochromism parameters and the Gutmann's acceptor numbers. The study indicates that solvatochromism is due to the contribution of solvent-to-cyanide hydrogen bonding and increased solvent dipolarity-polarizability. TD and TD-DFT calculations were performed on the ground and excited states of two different conformers of 2 and 4 to provide insight into the structural, electronic and optical properties of these systems.

Assessment of the differences in the phenolic composition and color characteristics of new strawberry (Fragaria x ananassa Duch.) cultivars by HPLC-MS and Imaging Tristimulus Colorimetry.

The phenolic composition (by HPLC-DAD-MS) and color characteristics (by Imaging Tristimulus Colorimetry) of four strawberry cultivars that have shown good climate adaptation to subtropical area (Nikte, Zamorana, Jacona and Pakal) have been assessed. 24 monomeric phenolics were identified, including 15 anthocyanins, 5 phenolic acids, 1 flavanol and 4 flavonols. Nikte and Zamorana showed the highest phenolic potential mainly due to their higher content of anthocyanins, while Pakal was richer in phenolic acids. Regarding color, Nikte and Zamorana were the more similar cultivars having the lowest values of lightness and hue. On the contrary, the color of Pakal was quite different from all the rest, due to the specific distribution between pelargonidin and cyanidin. The inclusion of both phenolic and colorimetric information in the Linear Discriminant Analysis allowed reaching very good discriminations among cultivars.