Effect of Facial Encumbrance on Excimer Formation and Charge Resonance Stabilization in Model Bichromophoric Assemblies

Excimer formation and charge resonance stabilization in covalently linked bichromophoric systems with flexible spacers are important processes relevant to biochemistry and functional materials. Requiring a π-stacked cofacial arrangement of a pair of aromatic molecules at a van der Waals contact, the underlying geometrical reorganization that accompanies these events continues to be debated. Here we use a variety of methods including two-color resonant two-photon ionization spectroscopy (2CR2PI), ion yield measurements, hole-burning spectroscopy (HB), and laser-induced fluorescence (LIF) excitation and emission spectroscopy to compare the gas-phase spectroscopy and dynamics of the van der Waals dimers of fluorene, 9-methylfluorene (MF), and 9,9′-dimethylfluorene (F1). The goal of this work is to probe the influence of methyl substitution on the dynamics of excimer formation and charge resonance (CR) stabilization. The fluorene dimer, (F)2, displays lifetime broadened electronic spectra and the dominance of excimer emission, consistent with a rapid (picoseconds) formation of a π-stacked excimer upon electronic excitation. Ion yield measurements of (F)2 reveal a lowering of the ionization potential (IP) by some 0.38 eV relative to the monomer, reflecting significant CR stabilization. These trends are mirrored in the 9-methylfluorene dimer, (MF)2, as one face of the π-system remains open. In contrast, the electronic spectrum of the dimethyl-substituted dimer, (F1)2, shows narrow features representing a single band system, and analysis of the torsional structure in dispersed fluorescence spectra identifies this as emission from the locally excited state of a tilted (non-π-stacked) dimer, with no evidence of excimeric emission. The structure of this dimer reflects the increased importance of C–H/π interactions in the dimethyl-substituted system, as increased steric constraints block a cofacial approach. The IP of (F1)2 shows CR stabilization which is roughly 1/2 of that in π-stacked (F)2 dimer. Extensive theoretical calculations support these findings and show the importance of sandwich-type configurations for excitonic delocalization and CR stabilization

Line Strengths of Rovibrational and Rotational Transitions in the X2Π^2\Pi Ground State of OH

A new line list including positions and absolute intensities (in the form of Einstein $A$ values and oscillator strengths) has been produced for the OH ground X\DP\ state rovibrational (Meinel system) and pure rotational transitions. All possible transitions are included with v\primed and v\Dprimed up to 13, and $J$ up to between 9.5 and 59.5, depending on the band. An updated fit to determine molecular constants has been performed, which includes some new rotational data and a simultaneous fitting of all molecular constants. The absolute line intensities are based on a new dipole moment function, which is a combination of two high level ab initio calculations. The calculations show good agreement with an experimental v=1 lifetime, experimental $\mu_\mathrm{v}$ values, and $\Delta$v=2 line intensity ratios from an observed spectrum. To achieve this good agreement, an alteration in the method of converting matrix elements from Hund's case (b) to (a) was made. Partitions sums have been calculated using the new energy levels, for the temperature range 5-6000 K, which extends the previously available (in HITRAN) 70-3000 K range. The resulting absolute intensities have been used to calculate O abundances in the Sun, Arcturus, and two red giants in the Galactic open and globular clusters M67 and M71. Literature data based mainly on [O I] lines are available for the Sun and Arcturus, and excellent agreement is found.Comment: 17 pages, 8 figues. 7 supplementary files: dipole moment functions (OH-X-DMFs.txt), equilibrium constants (OH-X-Equilibrium_Constants.txt), partition function (OH-X-Q_5-6000K.dat), PGOPHER file with molecular constants and transition matric elements (OH-XX.pgo), vibrational Einstein A and f values (OH-XX-Avv_fvv.txt), line list (OH-XX-Line_list.txt), and OH-Transformation_Equation_Extra.doc

Efficient singular-value decomposition of the coupled-cluster triple excitation amplitudes

We demonstrate a novel technique to obtain singular-value decomposition (SVD) of the coupled-cluster triple excitations amplitudes, $t_{ijk}^{abc}$. The presented method is based on the Golub-Kahan bidiagonalisation strategy and does not require $t_{ijk}^{abc}$ to be stored. The computational cost of the method is comparable to several CCSD iterations. Moreover, the number of singular vectors to be found can be predetermined by the user and only those singular vectors which correspond to the largest singular values are obtained at convergence. We show how the subspace of the most important singular vectors obtained from an approximate triple amplitudes tensor can be used to solve equations of the CC3 method. The new method is tested for a set of small and medium-sized molecular systems in basis sets ranging in quality from double- to quintuple-zeta. It is found that to reach the chemical accuracy ($\approx 1$ kJ/mol) in the total CC3 energies as little as $5-15\%$ of SVD vectors are required. This corresponds to the compression of the $t_{ijk}^{abc}$ amplitudes by a factor of ca. $0.0001-0.005$. Further benchmarks are performed to check the behaviour of the method in calculation of, e.g. interaction energies or rotational bariers, as well as in bond-breaking processes

Training Future Engineers to Be Ghostbusters: Hunting for the Spectral Environmental Radioactivity

Although environmental radioactivity is all around us, the collective public imagination often associates a negative feeling to this natural phenomenon. To increase the familiarity with this phenomenon we have designed, implemented, and tested an interdisciplinary educational activity for pre-collegiate students in which nuclear engineering and computer science are ancillary to the comprehension of basic physics concepts. Teaching and training experiences are performed by using a 4" x 4" NaI(Tl) detector for in-situ and laboratory {\gamma}-ray spectroscopy measurements. Students are asked to directly assemble the experimental setup and to manage the data-taking with a dedicated Android app, which exploits a client-server system that is based on the Bluetooth communication protocol. The acquired {\gamma}-ray spectra and the experimental results are analyzed using a multiple-platform software environment and they are finally shared on an open access Web-GIS service. These all-round activities combining theoretical background, hands-on setup operations, data analysis, and critical synthesis of the results were demonstrated to be effective in increasing students' awareness in quantitatively investigating environmental radioactivity. Supporting information to the basic physics concepts provided in this article can be found at http://www.fe.infn.it/radioactivity/educational

New Insights into the Charge-Transfer-to-Solvent Spectrum of Aqueous Iodide: Surface versus Bulk.

Liquid phase charge-transfer-to-solvent (CTTS) transitions are important, as they serve as photochemical routes to solvated electrons. In this work, broadband deep-ultraviolet electronic sum frequency generation (DUV-ESFG) and two-photon absorption (2PA) spectroscopic techniques were used to assign and compare the nature of the aqueous iodide CTTS excitations at the air/water interface and in bulk solution. In the one-photon absorption (1PA) spectrum, excitation to the 6s Rydberg-like orbital (5p → 6s) gives rise to a pair of spin-orbit split iodine states, 2P3/2 and 2P1/2. In the 2PA spectra, the lower-energy 2P3/2 peak is absent and the observed 2PA peak, which is ∼0.14 eV blue-shifted relative to the upper 2P1/2 CTTS peak seen in 1PA, arises from 5p → 6p electronic promotion. The band observed in the ESFG spectrum is attributed to mixing of excited states involving 5p → 6p and 5p → 6s promotions caused by both vibronic coupling and the external electric field generated by asymmetric interfacial solvation

Advanced Materials for Organic Photonics

V oblasti nových nízkomolekulárních organických materiálů patří deriváty difenyldiketopyrrolopyrrolu (DPP), používané dříve jako barviva a pigmenty, k objektům vysokého zájmu pro jejich potencionální aplikace v moderních technologiích. Studium jejich optických vlastností ve vztahu k jejich chemické struktuře umožní využití jejich vysokého potenciálu ve vývoji pokročilých inteligentních materiálů. Přehled chemických a fyzikálních vlastností DPP derivátů a zhodnocení současného stavu řešené problematiky jsou uvedeny v teoretické části této práce. Tři hlavní procesy studované v této práci jsou: klasická absorpce a emise, dvoufotonová absorpce (TPA) a zesílená spontánní emise (ASE). Výsledky budou diskutovány a shrnuty ve dvou částech: první zahrnuje první dvě výše zmíněné oblasti a druhá problematiku zesílené spontánní emise.Among low molecular organic materials, diphenyl-diketo-pyrrolopyrrole (DPP) derivatives used earlier as dyes are of high interest in modern technologies. The study of their optical properties related to their chemical structure will provide more information on the later relationship and comfort the high potential of DPP derivatives in the making of more performant smart materials. An overview of their chemical and physical properties is described in the theoretical part and followed by the state of the art in the field of interest concerning this thesis. The three main processes studied in this work are: The classic absorption and emission, the two photon absorption (TPA) and the amplified spontaneous emission (ASE). The results will be discussed and summarized in two parts: The first concerning the one and the two photon absorption and the second the amplified spontaneous emission.

On the relation between the echo-peak shift and Brownian-oscillator correlation function

We show that for systems that exhibit bimodal dynamics in their system-bath correlation function the shift of the stimulated photon-echo maximum as a function of waiting time reflects fairly well the long time part of the correlation function. For early times this correspondence breaks down due to a fundamentally different behaviour of the echo-peak shift in this time domain and because of the effect of finite pulse duration on the echo-peak shift. The method is used to characterize the solvation dynamics in various dye solutions.