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Excited-state descriptors based on the one-particle transition density matrix referring to the exciton picture have been implemented for time-dependent density functional theory. State characters such as local, extended pp*, Rydberg, or charge transfer can be intuitively classified by simple comparison of these descriptors. Strong effects of the choice of the exchange-correlation kernel on the physical nature of excited states can be found and decomposed in detail leading to a new perspective on functional performance and the design of new functionals. [ABSTRACT FROM AUTHOR]

The synthesis of a doubly bridged tolane is reported. The target is obtained in a five‐step synthesis, starting from commercially available 2‐amino‐meta‐xylene by a combination of a Sandmeyer reaction, radical bromination, and Stille‐type coupling, followed by double ring closing. The doubly tethered tolane is crystalline; the two phenyl rings are highly twisted with respect to each other both in solution and in the solid state. Optical spectroscopy and quantum chemical calculations show that the doubly bridged tolane is twisted not only in the ground state, but also in the excited state, leading to emission from the twisted state in solution and in the solid state. Strong phosphorescence is observed at cryogenic temperatures. Let's twist again: Two tethers fix the two phenyl rings of the target structure, a tolane, in a twisted fashion—even in the electronically excited state. The double bridging is necessary because a single linker is not sufficient to hold the two phenyl rings perpendicular to each other in the excited state. [ABSTRACT FROM AUTHOR]

The applicability and limitations of the restricted virtual space (RVS) approximation within the algebraic-diagrammatic construction (ADC) scheme for the polarization propagator up to third order is evaluated. In RVS-ADC, not only the core but also a substantial amount of energetically high-lying virtual orbitals is restricted in excitation energy calculations of low-lying excited electronic states. Using octatetraene, indole, and pyridine as representative examples and different standard basis sets of triple-zeta quality, RVS-ADC(2) turns out to be highly useful and to have negligible effects on ππ* excited states. However, for nπ* or πσ* states, the RVS approximation is generally less reliable but better at third-order than second-order ADC level. In addition, a unified, basis-set independent, thus normalized virtual orbital threshold (value) is introduced, making the RVS approximation more controllable and a priori applicable. © 2017 Wiley Periodicals, Inc. [ABSTRACT FROM AUTHOR]

The excited states of fac-tris(phenylpyridinato)iridium[Ir(ppy)3] and the smaller model complex Ir(C3H4N)3are computed using a number of high-levelab initio methods, including the recently implemented algebraic diagrammaticconstruction method to third-order ADC(3). A detailed descriptionof the states is provided through advanced analysis methods, whichallow a quantification of different charge transfer and orbital relaxationeffects and give extended insight into the many-body wave functions.Compared to the ADC(3) benchmark an unexpected striking differenceof ADC(2) is found for Ir(C3H4N)3, which derives from an overstabilization of charge transfer effects.Time-dependent density functional theory (TDDFT) using the B3LYP functionalshows an analogous but less severe error for charge transfer states,whereas the ωB97 results are in good agreement with ADC(3).Multireference configuration interaction computations, which are inreasonable agreement with ADC(3), reveal that static correlation doesnot play a significant role. In the case of the larger Ir(ppy)3complex, results at the TDDFT/B3LYP and TDDFT/ωB97levels of theory are presented. Strong discrepancies between the twofunctionals, which are found with respect to the energies, characters,as well as the density of the low lying states, are discussed in detailand compared to experiment. [ABSTRACT FROM AUTHOR]