Stability of dibromo-dipyrromethene complexes coordinated with B, Zn, and Cd in solutions of various acidities

The spectral luminescent properties of dipyrromethenates halogenated with bromine on both ends of the long axis and coordinated using boron fluoride, zinc, or cadmium in neutral ethanol and acidified with hydrochloric acid solutions were studied. The constants of the acid–base equilibrium of the complexes in the proton-donor solvents in the ground and excited states was determined. The mechanisms of complex protonation were discussed, depending on the structure of the compounds. The electronic structures of the neutral and protonated compounds were modeled and analyzed based on the quantum-chemical method. The structures and spectral-luminescence properties were calculated using the SMD model of ethanol solvent using the TD-DFT theory with the B3LYP functional and the composite def2-SVP/def2-TZVP/def2-TZVPP_ECP basis sets, depending on the atomic number of the elements

Photonics of halogenated zinc(II) and cadmium(II) dipyrromethene complexes

This article compares spectroscopic properties of the series of dipyrromethene dyes, namely their complexes of boron (III), zinc(II) and cadmium(II) with the halogenated ligands of the same structure. Absorption and emission spectra, lifetimes of long-lived emission and quantum yields of luminescence were studied as the functions of molecular structure of dipyrromethene complexes. The role of the position and nature of a substituent in a ligand, polarity of a solvent and temperature of media were also investigated. The studies demonstrate that replacing the central atom boron(III) by zinc(II) decreases the fluorescence quantum yield, indicating the increased role of non-radiative processes in excitation energy deactivations such as intersystem crossings. In addition, according to the heavy atom effect, the efficiency of intersystem crossings in halogen-substituted zinc(II) and cadmium(II) dipyrromethene complexes is higher than in the corresponding boron fluoride dipyrromethenes (BODIPY), which leads to increase in phosphorescence at low temperatures (frozen solutions). The obtained results make it possible to carry out further investigations of potential sensory properties that are required for systematic use of halogenated dipyrromethene complexes for the creation of modern optical oxygen sensors and singlet oxygen photosensitizers for photodynamic therapy or photocatalytic oxidative reactions

Photonics of boron fluoride and zinc dipyrromethene complexes

Spectral, photophysical, photochemical characteristics for mononuclear and binuclear dipyrromethenes in complexes with BF2 (BODIPY), bis-BODIPY and bis-helicates ([Zn2(L)2]) are described. The role of substituents (type and location in the ligand) and the medium in which dipyrromethene complexes are placed (solvents, solid-state matrices), the effect of different complexing agents (p- and d-elements) on the photonics of the complexes are discussed. The results of studying the lasing and photochemical properties of complexes under the action of laser irradiation are presented. In addition, for the described complexes the stability in the ground and excited states in protic media are estimated. Based on the analysis of the results discussed possibilities of practical application of these compounds to creating various optical devices

Photonics and application of dipyrrinates in the optical devices

In this paper spectral-luminescent, lasing, photochemical, and sensory characteristics of a number of Zn(II) and B(III) coordination complexes with dipyrrinates with different structures are presented. We have discussed relations of the structure of investigated compounds and formed solvates with their optical characteristics. The results showed that alkyl substituted dipyrrinates derivatives have excellent luminescent characteristics and demonstrated effective lasing upon excitation of Nd:YAG-laser. They can be used as active media for liquid tunable lasers. Zinc and boron fluoride complexes of dipyrrinates with heavy atoms in structure don't have fluorescence but have long-lived emission due to increased nonradiative intersystem processes in the excited state by the mechanism of a heavy atom. For solid samples based on halogenated complexes was found dependency of the long-lived emission intensity of the oxygen concentration in gas flow. The presence of line segment indicates the possibility of the use of these complexes as a basis for creation of optical sensors for oxygen. Moreover, results of a study of halogen-substituted aza-complexes under irradiation are presented. Such complexes are promising for the creating media for generation of singlet oxygen (1O2), which is important for photodynamic therapy in medicine and photocatalytic reactions in the industry

A roadmap for the conservation of freshwater mussels in Europe

Europe has a long history of human pressure on freshwater ecosystems. As pressure continues to grow and new threats emerge, there is an urgent need for conservation of freshwater biodiversity and its ecosystem services. However, whilst some taxonomic groups, mainly vertebrates, have received a disproportionate amount of attention and funds, other groups remain largely off the public and scientific radar. Freshwater mussels (Bivalvia, Unionida) are an alarming example of this conservation bias and here we point out six conceptual areas that need immediate and long-term attention: knowledge, threats, socioeconomics, conservation, governance and education. The proposed roadmap aims to advance research, policy and education by identifying the most pressing priorities for the short- and long-term conservation of freshwater mussels across Europe.COST - European Cooperation in Science and Technology(CA18239