Understanding Perceptions of Problematic Facebook Use: When People Experience Negative Life Impact and a Lack of Control

While many people use social network sites to connect with friends and family, some feel that their use is problematic, seriously affecting their sleep, work, or life. Pairing a survey of 20,000 Facebook users measuring perceptions of problematic use with behavioral and demographic data, we examined Facebook activities associated with problematic use as well as the kinds of people most likely to experience it. People who feel their use is problematic are more likely to be younger, male, and going through a major life event such as a breakup. They spend more time on the platform, particularly at night, and spend proportionally more time looking at profiles and less time browsing their News Feeds. They also message their friends more frequently. While they are more likely to respond to notifications, they are also more likely to deactivate their accounts, perhaps in an effort to better manage their time. Further, they are more likely to have seen content about social media or phone addiction. Notably, people reporting problematic use rate the site as more valuable to them, highlighting the complex relationship between technology use and well-being. A better understanding of problematic Facebook use can inform the design of context-appropriate and supportive tools to help people become more in control.Comment: CHI 201

Exceptionally Long-Lived Photodriven Multi-Electron Storage without Sacrificial Reagents

Photoexcitation of a molecular pentad in the presence of Sc3+ in de-aerated CH3CN leads to a quinone dianion that is stable on the millisecond timescale. Light-driven electron accumulation on the quinone unit is sensitized by two Ru(bpy)32+ complexes in an intramolecular process, which relies on covalently attached triarylamine donors rather than on sacrificial reagents. Lewis acid–Lewis base interactions between Sc3+ and quinone dianion are responsible for the exceptionally long lifetime of this photoproduct. Our study of photoinduced multi-electron transfer is relevant in the greater context of solar energy conversion

Electron Transfer Rate Maxima at Large Donor−Acceptor Distances

Because of their low mass, electrons can transfer rapidly over long (>15 Å) distances, but usually reaction rates decrease with increasing donor–acceptor distance. We report here on electron transfer rate maxima at donor–acceptor separations of 30.6 Å, observed for thermal electron transfer between an anthraquinone radical anion and a triarylamine radical cation in three homologous series of rigid-rod-like donor–photosensitizer–acceptor triads with p-xylene bridges. Our experimental observations can be explained by a weak distance dependence of electronic donor–acceptor coupling combined with a strong increase of the (outer-sphere) reorganization energy with increasing distance, as predicted by electron transfer theory more than 30 years ago. The observed effect has important consequences for light-to-chemical energy conversion

Reaction Rate Maxima at Large Distances between Reactants

One commonly thinks that two reactants need to come very close to one another in order for a chemical reaction to occur. This is true for most reaction types, but electron transfer is an exception in this regard. It is a well-documented fact that electron transfers can occur over long distances (≥15 Å), but it is much less well-known that theory predicts a regime in which electron transfer rates in crease with increasing distance between reactants. This contribution explains the physical origin of this counter-intuitive behavior, and it identifies a set of conditions that might facilitate its experimental observation

Unusual Distance Dependences of Electron Transfer Rates

Usually the rates for electron transfer (kET) decrease with increasing donor–acceptor distance, but Marcus theory predicts a regime in which kET is expected to increase when the transfer distance gets longer. Until recently, experimental evidence for such counter-intuitive behavior had been very limited, and consequently this effect is much less well-known than the Gaussian free energy dependence of electron transfer rates leading to the so-called inverted driving-force effect. This article presents the theoretical concepts that lead to the prediction of electron transfer rate maxima at large donor–acceptor distances, and it discusses conditions that are expected to favor experimental observations of such behavior. It continues with a consideration of specific recent examples in which electron transfer rates were observed to increase with increasing donor–acceptor distance, and it closes with a discussion of the importance of this effect in the context of light-to-chemical energy conversion

Gauge boson couplings at LEP

A review is given of the measurements of triple and quartic couplings among the electroweak gauge bosons performed at LEP by the four experiments ALEPH, DELPHI, L3 and OPAL. Emphasis is placed on recently published results and on combinations of results performed by the LEP electroweak gauge-couplings group. All measurements presented are consistent with the Standard Model expectations.Comment: 6 pages, 7 figures. To be published in the proceedings of the BEACH04 conference, Chicago, June 27-July 3 200

Light-Driven Electron Accumulation in a Molecular Pentad

Accumulation and temporary storage of redox equivalents with visible light as an energy input is of pivotal importance for artificial photosynthesis because key reactions, such as CO2 reduction or water oxidation, require the transfer of multiple redox equivalents. We report on the first purely molecular system, in which a long-lived charge-separated state (τ≈870 ns) with two electrons accumulated on a suitable acceptor unit can be observed after excitation with visible light. Importantly, no sacrificial reagents were employed

Influence of Donor-Acceptor Distance Variation on Photoinduced Electron and Proton Transfer in Rhenium(I)-Phenol Dyads

A homologous series of four molecules in which a phenol unit is linked covalently to a rhenium(I) tricarbonyl diimine photooxidant via a variable number of p-xylene spacers (n = 0–3) was synthesized and investigated. The species with a single p-xylene spacer was structurally characterized to get some benchmark distances. Photoexcitation of the metal complex in the shortest dyad (n = 0) triggers release of the phenolic proton to the acetonitrile/water solvent mixture; a H/D kinetic isotope effect (KIE) of 2.0 ± 0.4 is associated with this process. Thus, the shortest dyad basically acts like a photoacid. The next two longer dyads (n = 1, 2) exhibit intramolecular photoinduced phenol-to-rhenium electron transfer in the rate-determining excited-state deactivation step, and there is no significant KIE in this case. For the dyad with n = 1, transient absorption spectroscopy provided evidence for release of the phenolic proton to the solvent upon oxidation of the phenol by intramolecular photoinduced electron transfer. Subsequent thermal charge recombination is associated with a H/D KIE of 3.6 ± 0.4 and therefore is likely to involve proton motion in the rate-determining reaction step. Thus, some of the longer dyads (n = 1, 2) exhibit photoinduced proton-coupled electron transfer (PCET), albeit in a stepwise (electron transfer followed by proton transfer) rather than concerted manner. Our study demonstrates that electronically strongly coupled donor–acceptor systems may exhibit significantly different photoinduced PCET chemistry than electronically weakly coupled donor–bridge–acceptor molecules