Quantum reality with negative-mass particles.

Physical interpretations of the time-symmetric formulation of quantum mechanics, due to Aharonov, Bergmann, and Lebowitz are discussed in terms of weak values. The most direct, yet somewhat naive, interpretation uses the time-symmetric formulation to assign eigenvalues to unmeasured observables of a system, which results in logical paradoxes, and no clear physical picture. A top-down ontological model is introduced that treats the weak values of observables as physically real during the time between pre- and post-selection (PPS), which avoids these paradoxes.

Some Notes on Counterfactuals in Quantum Mechanics.

Counterfactuals, i.e., events that could have occurred but eventually did not, play a unique role in quantum mechanics in that they exert causal effects despite their non-occurrence.

Interaction-free ghost-imaging of structured objects.

Quantum - or classically correlated - light can be employed in various ways to improve resolution and measurement sensitivity. In an "interaction-free" measurement, a single photon can be used to reveal the presence of an object placed within one arm of an interferometer without being absorbed by it. With a technique known as "ghost-imaging", entangled photon pairs are used for detecting an opaque object with significantly improved signal-to-noise ratio while preventing over-illumination.

The Weak Reality That Makes Quantum Phenomena More Natural: Novel Insights and Experiments.

While quantum reality can be probed through measurements, the Two-State Vector Formalism (TSVF) reveals a subtler reality prevailing between measurements. Under special pre- and post-selections, odd physical values emerge. This unusual picture calls for a deeper study.

Interaction-Free Effects Between Distant Atoms.

A Gedanken experiment is presented where an excited and a ground-state atom are positioned such that, within the former's half-life time, they exchange a photon with 50% probability. A measurement of their energy state will therefore indicate in 50% of the cases that no photon was exchanged. Yet other measurements would reveal that, by the mere possibility of exchange, the two atoms have become entangled.

The Case of the Disappearing (and Re-Appearing) Particle.

A novel prediction is derived by the Two-State-Vector-Formalism (TSVF) for a particle superposed over three boxes. Under appropriate pre- and post-selections, and with tunneling enabled between two of the boxes, it is possible to derive not only one, but three predictions for three different times within the intermediate interval. These predictions are moreover contradictory.

Entrapped energy in chiral solutions: quantification and information capacity.

A homogeneous solution of a chiral substance stores a residual chemical potential, related to its overall anisotropy. Therefore, by mixing solutions of opposite enantiomers, heat release may take place, corresponding to the mutual anisotropy annulment. In the following study we present proofs for this fundamental, yet unexplored, prediction by measuring the heat released upon mixing of aqueous solutions of D-proline with L-proline, as well as D-alanine with L-alanine, using isothermal titration calorimetry.

Ortho-para spin isomers of the protons in the methylene group--possible implications for protein structure.

The two hydrogen atoms attached to the carbon in the methylene group are of two different spin configurations, similar to those in the case of water: ortho, where the two proton spins are parallel to each other, and para, where they are antiparallel. The ortho configuration has three degenerate states, while the para configuration is singular, leading to a statistical ratio of these isomers 3:1 ortho/para. Such spin isomers are present in glycine and most chiral amino acids where they may induce broadening of structural zones, a possibility which remains to be assessed.

Subtle differences in structural transitions between poly-L- and poly-D-amino acids of equal length in water.

Mirror-image asymmetric molecules, i.e., chiral isomers or enantiomers, are classically considered as chemically identical.