No abstract

Europium beta diketonates are easily synthesized highly luminescent complexes with high temperature sensitivity. We report on the temperature dependence of the luminescence of recently synthesized europium complexes originally prepared for use as light emitting diodes. It has been discovered that when incorporated in a polymer matrix, their decay lifetime can provide accurate measurement of temperature. Their lifetime as a function of temperature depends on three factors: (i) the type and number of ligands in the complex, (ii) the particular polymer used for the matrix, and (iii) the europium chelate to polymer matrix concentration ratio. Various tris and tetrakis europium chelates are used to study ligand effects, while the polymers FIB, polycarbonate, and Teflon© are used to analyze matrix effects. In all cases studied, higher concentrations give rise to shorter lifetimes and higher temperature sensitivities, with sensitivity defined as ΔI/(IrefΔT). We propose to explain this phenomenon by using the following equation: 1/τobs≡Ktotal=kr+knr(T)+kc([Eu]). Here Ktotal is the observed decay rate, which is the inverse of the observed lifetime, while kr and knr(T) are the radiative and nonradiative decay rates, respectively. As well as being dependent on temperature, knr(T) for these complexes is very dependent on the environment, i.e., solvent or polymer, and can be considered as ken(T). The rate kc([Eu]) is the quenching term dependent on the concentration of the europium complex.

We report new divalent osmium complexes that feature strong red metal-to-ligand-charge-transfer (MLCT) phosphorescence and electrophosphorescence. The general formula of the complexes is Os(II)(N-N)(2)L-L, where N-N is either a bipyridine or a phenanthroline and L-L is either a phosphine or an arsine. New polypyridyl ligands synthesized are 4,4'-di(biphenyl)-2,2'-bipyridine (15) and 4,4'-di(diphenyl ether)-2,2'-bipyridine (16), and the 1,10-phenanthroline derivatives synthesized are 4,7-bis(p-methoxyphenyl)-1,10-phenanthroline (17), 4,7-bis(p-bromophenyl)-1,10-phenanthroline (18), 4,7-bis(4'-phenoxybiphen-4-yl)-1,10-phenanthroline (19), and 4,7-bis(4-naphth-2-ylphenyl)-1,10-phenanthroline (20). 4,4'-Diphenyl-2,2'-bipyridine (21) and 4,7-diphenyl-1,10-phenanthroline (22) were also used in these studies. Strong pi-acid ligands used were 1,2-bis(diphenylarseno)ethane (23), cis-1,2-bis(diphenylphosphino)ethylene (24), and cis-1,2-vinylenebis(diphenylarsine) (25). Ligand 25 is used for the first time in these types of luminescent osmium complexes. These compounds feature strong MLCT absorption bands in the visible region and strong red phosphorescent emission ranging from 611 to 651 nm, with quantum efficiency up to 45% in ethanol solution at room temperature. Red organic light-emitting diodes (OLEDs) were successfully fabricated by doping the Os(II) complexes into blend of poly(N-vinylcarbazole) (PVK) and 2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PBD). Brightness over 1400 cd/m(2) for a double-layer device has been reached, with a turn-on voltage of 8 V. The maximum external quantum efficiency was 0.64%. Commission Internationale de l'Eclairage (CIE) chromaticity coordinates (x, y) of the red electrophosphorescence from the complexes are (0.65, 0.34), which indicates pure red emission.

This paper investigates how financial sector leverage affects macroeconomic instability and welfare. In the model, banks borrow (use leverage) to allocate resources to productive projects and pro vide liquidity. When banks do not actively issue new equity, aggregate outcomes depend on the level of equity in the financial sector. Equilibrium is inefficient because agents do not internalize how their decisions affect volatility, aggregate leverage, and the returns on assets. Leverage creates systemic risk, which increases the frequency and duration of crises. Limiting leverage decreases asset price volatility and increases expected returns, which decrease the likelihood that the financial sector is undercapitalized. (JEL E32, E44, G01, G21)

Application of bis(propylenedioxythiophene) (bis(ProDOT)) π-conjugated bridges bearing alkyl or aryl substituents in electro-optic (EO) chromophores is presented. A series of three bis(ProDOT)-based chromophores and a bithiophene-based control chromophore were prepared and fully characterized with regard to EO applications. The highly planar bis(ProDOT) bridge results in slightly larger (∼10%) molecular hyperpolarizability ( ) values as compared to the bithiophene bridge, as measured by hyperRayleigh scattering at a variety of wavelengths. In amorphous polycarbonate guest-host films, however, the bulky substituents on the bis(ProDOT) bridge result in significantly larger (∼70%) poling-induced EO coefficient (r 33 ) values, as measured by simple reflection ellipsometry at 1310 nm. This can be attributed to a roughly 2-fold enhancement in poling efficiency due to reduced intermolecular dipole-dipole interactions. This chromophore architecture also exhibits excellent temporal alignment stability and photochemical stability as compared to benchmark AJL8, FTC, and CLD chromophore systems. Incorporation of the strong CF 3 -phenyl-substituted tricyano-furan (TCF) acceptor into a bis(ProDOT)-based chromophore resulted in a zzz (-2ω;ω,ω) value at 1907 nm of 5700 ( 400 × 10 -30 esu and an r 33 value of 69 ( 14 pm/V at 32.8 total chromophore weight %.