Electronic Energy Transfer in a Single Donor–Acceptor Pair with Triplet–Triplet Absorption

Optics and Spectroscopy - The protocol of dynamic decoupling using a sequence of resonance RF pulses with different shapes in a system of dipole-coupled electron/nuclear spins with inhomogeneous...     

Probabilistic Controlled Teleportation of a Triplet W State

A scheme for probabilistic controlled teleportation of a triplet W state from the sender Alice to the distant receiver Bob is proposed. In this scheme, an m-qubit GHZ state serves as the control parameter. The m control qubits are shared by m（s1, s2… sm） spatially-separated supervisors. With the aid of local operations and individual measurements, including Bell-state measurement, Von Neumann measurement, and mutual classical communication, etc., Bob can faithfully reconstruct the original state by performing relevant unitary transformations. However, even if one participant does not cooperate during the process, the receiver Bob cannot fully recover the original state. This protocol can be extended to probabilistic controlled teleportation of an arbitrary N-qubit state and some other N-qubit entangled states.     

Triplet‐Triplet Electron Excitation Energy Transfer in the Gas Phase for the Carbazol–Diacetyl Donor‐Acceptor Pair

For the carbazol–diacetyl donoracceptor pair, the features of exothermal triplettriplet (TT) transfer of electron excitation energy in the gas phase upon excitation of carbazol by the nitrogen laser radiation which is not absorbed by diacetyl have been investigated. The luminescence spectra of carbazol in the gas phase have been studied. It is shown that carbazol phosphorescence in the gas phase is absent. Therefore, for estimating the TT transfer efficiency and its temperature dependence, in the kinetic approximation the dependences of the intensity of timeresolved delayed fluorescence of carbazol and sensitized phosphorescence of diacetyl on diacetyl pressure have been analyzed. It has been found that in the gas phase the features of the electronic structure of the molecules under investigation are responsible for the low efficiency of transfer (2·10^–4 at 453 K), which increases by an order of magnitude with increasing temperature in the 453–513 K range despite the increasing influence of the back transfer.     

Relativistic Jahn–Teller Effect for Triplet States of Tetrahedral Molecular Complexes

A relativistic multimode Jahn?Teller effect for tetrahedral molecular complexes in a triplet electronic state is considered. The analysis is based on the symmetry properties of the electronic Hamiltonian and its generalized symmetry operators, acting on both the coordinates (spatial operations) and spins (matrix operations) of the electrons. As a result, a 9 × 9 vibronic matrix that includes the vibronic coupling constants of orbital and spin-orbital nature and depends on the five normal modes of t₂ and e symmetry has been obtained.     

Quantum MIMO Communication Scheme Based on Quantum Teleportation with Triplet States

A novel quantum MIMO communication scheme is proposed by generalizing the wireless communication technique to the quantum field. The MIMO quantum teleportation can be implemented with triplet states in order to enhance the capacity and fidelity of the quantum channel, in which an n-qubit sequence of quantum signals can be transmitted through the MIMO quantum channel by applying the diversity technique. The quantum noise filtering is involved before the quantum signals are outputted. The analysis and discussions demonstrate that the quantum MIMO teleportation can be performed securely with high capacity and fidelity.     

Elastic Scattering of Ultracold ^133Cs and SSRb Atoms in Triplet State

Elastic scattering properties of the ultracold interaction for the triplet state of ^133Cs and ^85Rb atoms are studied using two kinds of potentials by the same phase Ф. One is the interpolation potential, and another is Lennard-Jones potential （LJl2,6 ）. The radial Schrodtinger equation is also solved using two computational methods, the semiclassical method （WKB）, and the Numerov method. Our results are found to be in an excellent agreement with the more recent theoretical values. It shows that the two potentials and methods are applicable for studying ultracold collisions between the mixing alkali atoms.     

Time-Resolved and Pulse EPR Study of Triplet States of Alkylketones in β-Cyclodextrin

The triplet states of deoxybenzoin (DOB) and benzophenone (BP) molecules in randomly methylated β-cyclodextrin (CD) cavity are studied by time-resolved (TR) and pulse electron paramagnetic resonance (EPR). The observed TR EPR spectrum of DOB in β-CD at 30 K is close to the spectrum measured in polar solvent trifluoroethanol, revealing strong hydration by water molecules. At the same time, TR EPR spectrum of BP in β-CD corresponds to nonpolar surrounding of the CO-group. The electron spin relaxation times T ₁ and T ₂ of triplet BP at 30 K measured by pulse EPR are found to be different in β-CD compared to nonpolar toluene glass. The observed increase of T ₂ by up to a factor of four in β-CD is caused by the lower vibration amplitude of CO-bond of BP due to the confinement in β-CD. The influence of β-CD with covalently attached nitroxide on the triplet states of DOB and BP is principally different: the excited triplet states could not be observed by TR EPR due to the efficient quenching of the excited states by nitroxide.     

The <Emphasis Type="Italic">N</Emphasis> = 1 Triplet Vertex Operator Superalgebras

We introduce a newfamily of C ₂-cofinite N = 1 vertex operator superalgebras , m ≥ 1, which are natural super analogs of the triplet vertex algebra family , p ≥ 2, important in logarithmic conformal field theory. We classify irreducible -modules and discuss logarithmic modules. We also compute bosonic and fermionic formulas of irreducible characters. Finally, we contemplate possible connections between the category of -modules and the category of modules for the quantum group , , by focusing primarily on properties of characters and the Zhu’s algebra . This paper is a continuation of our paper Adv. Math. 217, no.6, 2664–2699 (2008). The second author was partially supported by NSF grant DMS-0802962.     

Pulsed EPR and ENDOR on the Peridinin Triplet State Involved in the Photoprotective Mechanism in Peridinin–Chlorophyll a–Proteins

The photoexcited triplet state of the carotenoid peridinin in the peridinin–chlorophyll a–protein (PCP) of the dinoflagellate Heterocapsa pygmaea has been investigated by pulsed electron paramagnetic resonance (EPR) and pulsed electron-nuclear double resonance (ENDOR) spectroscopies. The α- and β-protons hyperfine couplings of the peridinin-conjugated chain have been derived from Davies and Mims ENDOR experiments. The spectroscopic results have been compared to those obtained for the main form of the PCP complex and for the high-salt PCP form from Amphidinium carterae. The EPR features of the peridinin triplet state are very similar in the antenna complexes belonging to the two different dinoflagellate species, proving that the triplet formation pathway and the triplet localization on one specific peridinin per subcluster are common features of different PCP antennas. No significant variation of the hyperfine couplings of the peridinin triplet state has been detected between the main form of the PCP complex from A. carterae and H. pygmaea. The spectroscopic results confirm the close relationship between the Amphidinium PCP and the corresponding Heterocapsa complex at least in terms of mutual arrangement of the chlorophyll a–peridinin pair involved in photoprotection and in terms of conformation of the peridinin-conjugated chain.     

Relaxation Processes and Coherent Spin Manipulations for Triplet Si–C Divacancies in Silicon Carbide Enriched Tenfold in the 13C Isotope

JETP Letters - Coherent spin manipulations of ensembles of color centers in the form of neutral VSi–VC divacancies with the spin $$S = 1$$ in hexagonal silicon carbide 6H–SiC enriched...     

Pulsed EPR Analysis of the Photo-Induced Triplet Radical Pair in the BLUF Protein SyPixD: Determination of the Protein–Protein Distance and Orientation in the Oligomeric Protein

A photo-induced radical pair of FADH^· and Y8^· and in BLUF protein SyPixD was studied by pulsed electron paramagnetic resonance (EPR) spectroscopy. Blue light illumination at 150 K for 30 min followed by cooling to 50 K during illumination induced the stable radical pair. The EPR signal has been characterized by a Pake doublet signal with complete S = 1 spin state. The radical pair was utilized as a probe to analyze the oligomer of SyPixD. The relative arrangement of PixD proteins in the complex was investigated by pulsed electron–electron double resonance (PELDOR) with the orientation selection. Based on the decameric structure in the crystal, the possible structure for the PELDOR results was discussed.