Synthesis and IR-Spectral Characterization of Mixed-Ligand Solid State Complexes of Some Lanthanoides with Mono-(2-ethylhexyl) Phosphoric Acid

The synthesis of a new type of complexes of Y, Nd and Er with mono-(2-ethylhexyl) phosphoric acid is reported. The elemental composition, IR-spectral data and thermogravimetric analysis prove the presence of both mono-and bivalent ions of the acid as ligands as well as of NO₃-ions. The IR-spectrum is interpreted in comparison with those of other lanthanoid complexes of the same acid.     

Optical shuttering action in nematic phase of SMHBLC: observation of a ribbon-like texture

In this study, complexes belonging to supramolecular hydrogen-bonded liquid crystal homologous series are synthesized and characterized. Hydrogen bond is formed between p-n-alkyloxy benzoic acids (nBAO, where n?=?5–11) and chlorobenzoic acid (ClBAO), respectively. The isolated homologues are characterized by various techniques such as polarizing optical microscopic (POM) studies, differential scanning calorimetry (DSC), and Fourier transform–infrared spectroscopy. Based on the POM and DSC studies, the phase diagram has been constructed and discussed. A new smectic ordering, labeled as smectic R, has been characterized, which exhibits a ribbon-like texture. This phase is observed in the complexes pertaining to the higher homologous series. Tilt angle in this phase has been experimentally deduced and the results are fitted to the power law which concurs with the mean-field theory predicted value. Optical shuttering action in the homologue has been detected in the nematic phase and the results are also discussed.     

Recollements of extension algebras

Let A be a finite-dimensional algebra over arbitrary base field k. We prove: if the unbounded derived module category D-(Mod-A) admits symmetric recollement relative to unbounded derived module categories of two finite-dimensional k-algebras B and C:D- (Mod - B) D-(Mod - A) D-(Mod - C),then the unbounded derived module category D-(Mod - T(A)) admits symmetric recollement relative to the unbounded derived module categories of T(B) and T(C):D-(Mod - T(B)) D-(Mod - T(A)) D-(Mod -T(C)).     

Extended X‐ray absorption fine structure and multiple‐scattering simulation of nickel dithiolene complexes Ni[S2C2(CF3)2]2n (n = −2, −1, 0) and an olefin adduct Ni[S2C2(CF3)2]2(1‐hexene)

A series of Ni dithiolene complexes Ni[S₂C₂(CF₃)]₂ⁿ (n = ?2, ?1, 0) ( 1 , 2 , 3 ) and a 1‐hexene adduct Ni[S₂C₂(CF₃)₂]₂(C₆H₁₂) ( 4 ) have been examined by Ni K‐edge X‐ray absorption near‐edge structure (XANES) and extended X‐ray absorption fine‐structure (EXAFS) spectroscopies. Ni XANES for 1 – 3 reveals clear pre‐edge features and approximately +0.7 eV shift in the Ni K‐edge position for `one‐electron' oxidation. EXAFS simulation shows that the Ni—S bond distances for 1 , 2 and 3 (2.11–2.16 Å) are within the typical values for square planar complexes and decrease by ～0.022 Å for each `one‐electron' oxidation. The changes in Ni K‐edge energy positions and Ni—S distances are consistent with the `non‐innocent' character of the dithiolene ligand. The Ni—C interactions at ～3.0 Å are analyzed and the multiple‐scattering parameters are also determined, leading to a better simulation for the overall EXAFS spectra. The 1‐hexene adduct 4 presents no pre‐edge feature, and its Ni K‐edge position shifts by ?0.8 eV in comparison with its starting dithiolene complex 3 . Consistently, EXAFS also showed that the Ni—S distances in 4 elongate by ～0.046 Å in comparison with 3 . The evidence confirms that the neutral complex is `reduced' upon addition of olefin, presumably by olefin donating the π‐electron density to the LUMO of 3 as suggested by UV/visible spectroscopy in the literature.     

Spectral Studies on Cyclic Chromotropic Acid Tetramers and Their Interaction with Metal Ions

Abstract

With comparable molar quantities, chromotropic acid reacts with compounds containing aldehyde groups -CHO e.g. with formadehyde or glyoxylic acid to form cyclic compounds with rings containing four chromotropic acid fragments — cyclotetrachromotropylene derivatives. The cyclic compounds, due to the presence of a cavity in the molecule, can play the part of host and complex smaller molecules, which has been confirmed on the basis of triethylamine by the ¹H-NMR measurements. Using spectrophotometric method the stability constant of 1:1 complex formed between Ti(IV) and cyclic compound chromotropic acid with formaldehyde has been determined - K = (9,0 ± 0,1) 10⁴.     

A note on Bridgeland Hall algebras

In this note, let 𝒜 be a finitary hereditary abelian category with enough projectives. By using the associativity formula of Hall algebras, we give a new proof of the main theorem in [17 Yanagida, S. (2016). A note on Bridgeland’s Hall algebra of two-periodic complexes. Math. Z. 282(3):973–991.[Crossref], [Web of Science ®] , [Google Scholar]], which states that the Bridgeland Hall algebra of 2-cyclic complexes of projective objects in 𝒜 is isomorphic to the Drinfeld double Hall algebra of 𝒜.     

Variable temperature Mössbauer spectroscopic studies of oxo-centered trinuclear mixed-valence iron succinate, mesaconate and isophthalate complexes

Three new oxo-centered trinuclear mixed-valence iron complexes, iron succinate, iron mesaconate and iron isophthalate have been prepared. Temperature dependent valence delocalization processes were observed for all the complexes on variable temperature Mössbauer spectroscopic studies. Two clear quadrupole split doublets attributed to high-spin Fe(III) and high-spin Fe(II) states were existed for the complexes at liquid nitrogen temperature. At room temperature a nearly averaged singlet peak was observed for mesaconate complex and averaged doublet peaks were observed for succinate and isophthalate complexes with IS values 0.68 and 0.68 mms^?1 and QS values 0.44 and 0.48 mms^?1 respectively.     

Photophysics of the Lanthanide Complexes with Conjugated Carboxylic Acids by Low Temperature Fluorescent Spectroscopy

In the context, some lanthanide (Eu³⁺, Tb³⁺ and Sm³⁺) complexes with conjugated carboxylic acids (pyridine-carboxylic acids derivatives) have been synthesized and characterized. The low temperature fluorescent spectra for these complexes have been measured at nitrogen atmosphere (77 K), indicating that the central Ln³⁺ ions locate in an equivalent coordination environment with low symmetry for most of these lanthanide complexes belonging to dimeric or polymeric structure. Therefore, the electronic dipole transition (supersensitive transition) (⁵D₀ → ⁷F₂ for Eu³⁺, ⁵D₄ → ⁷F₆ for Tb³⁺, ⁴G_5/2 → ⁶H_9/2 for Sm³⁺) and magnetic dipole transition (⁵D₀ → ⁷F₁ for Eu³⁺, ⁵D₄ → ⁷F₅ for Tb³⁺, ⁴G_5/2 → ⁶H_5/2 for Sm³⁺) show the regular change in the corresponding split number of fluorescent spectra, which can be realized to predict the fine structure of lanthanide complexes.     

Energy transfer from a polymer host to a europium complex in light-emitting diodes

Energy transfer leading to electroluminescence of a lanthanide complex, Eu(Fod)₃MK (Fod=heptafluoro-dimethyl-octanedionate, MK=4, 4′-bis(N,N-dimethylaminobenzophenone) doped into PVK host is investigated. The optical properties of pure Eu(Fod)₃MK and its doping in PVK show that the PVK host can efficiently transfer energy to europium ions through a co-ligand of MK due to good spectrally overlap. Light-emitting diodes (LED) consisting of PVK doped with 1-5 wt% of Eu(Fod)₃MK also demonstrates this energy transfer. Organolanthanide complexes doped into a wide-gap conducting polymers would lead to efficient and pure red organic LEDs to solve the full colour conjugated polymer displays.