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  • 1
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 94 (1972), S. 1119-1125 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 6780-6784 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: As an extension of our previous study on polarizabilities [J. Chem. Phys. 115, 1052 (2001)], we investigate the molecular third-order nonlinear optical properties, i.e., the second hyperpolarizabilities (γ), of three types of model oligomers (made of phenylene vinylenes), i.e., para-oligomers and meta-oligomers with fractal and nonfractal structures, which are considered to be models of dendron parts involved in Cayley-tree-type dendrimers. Similarly to the polarizability case, the chain-length dependence of γ of para-oligomers is found to be much larger than that of nonfractal meta-oligomers, while fractal meta-oligomers exhibit an intermediate chain-length dependency of γ between them. The spatial contributions of π-electrons to γ of these systems are elucidated using hyperpolarizability density analysis. It is found that the spatial contributions of π-electrons to γ of nonfractal meta-oligomers are much smaller than those of para-oligomers and are well decoupled at the meta-substituted benzene rings, while the fractal meta-oligomers show significantly large spatial contributions of π-electrons to γ in their linear-leg (para-substituted phenylene vinylene) regions similarly to the case of para-oligomers although the distributions are also well decoupled at the meta-substituted benzene rings. This feature supports the distinct features of chain-length dependency of γ for these oligomers. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Polyradicals comprised of m-phenylene-bridged organic radicals are well known as building blocks of organic ferromagnets, in which radical groups are connected with each other at the meta position in the benzene ring, and the parallel-spin configurations between radical sites are more stabilized than the antiparallel ones. Topological rules for spin alignments enable us to design organic high-spin dendrimers and polymers with the ferromagnetic ground states by linking various radical species through an m-phenylene unit. However, no systematic ab initio treatment of such spin dendrimers and magnetic polymers has been reported until now, though experimental studies on these materials have been performed extensively in the past ten years. As a first step to examine the possibilities of ferromagnetic dendrimers and polymers constructed of m-phenylene units with organic radicals, we report density functional and molecular orbital calculations of six m-phenylene biradical units with radical substituents and polycarbenes linked with an m-phenylene-type network. The relative stability between the spin states and spin density population are estimated by BLYP or B3LYP and Hartree–Fock calculations in order to clarify their utility for constructions of large spin denderimers and periodic magnetic polymers, which are final targets in this series of papers. It is shown that neutral polyradicals with an m-phenylene bridge are predicted as high-spin ground-state molecules by the computations, while m-phenylene-bridged ion-radical species formed by doping may have the low-spin ground states if zwitterionic configurations play significant roles to stabilize low-spin states. Ab initio computations also show an important role of conformations of polyradicals for stabilization of their high-spin states. The computational results are applied to molecular design of high-spin dendrimers and polymers. Implications of them are also discussed in relation to recent experimental results for high-spin organic molecules. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 1052-1059 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We investigate the size-dependency of static polarizabilities (α) (in the chain-length direction) of three types of model oligomers (made of phenylene vinylenes), i.e., para-oligomers and meta-oligomers with fractal and nonfractal structures by the finite-field method using molecular orbital calculations. The fractal-structured meta-oligomers are considered to be models of dendron parts involved in Cayley-tree-type dendrimers. The chain-length dependence of α of para-oligomers is found to be much larger than that of nonfractal-structured meta-oligomers, while the fractal-structured meta-oligomers exhibit an attractive chain-length dependence of α; the α values of meta-structured oligomers are near to those of nonfractal-structured meta-oligomers in small chain-length region, while they are close to those of para-oligomers in sufficiently large chain-length region. Using the polarizability density analysis, the spatial contributions of π-electrons to α of nonfractal-structured meta-oligomers are found to be smaller than those of para-oligomers and to be well decoupled at the meta-substituted benzene rings. In contrast, it is found that the spatial contributions of π-electrons to α in linear-leg regions for fractal-structured meta-oligomers are similar to those for the para-oligomers though the α density distributions for fractal-structured meta-oligomers are also well decoupled at the meta-substituted benzene rings. Such features, which reflect the fractal structure, is predicted to cause the attractive size-dependency of α for fractal-structured meta-oligomers. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: As a first step toward examination of ferromagnetic polymers and dendrimers by ab initio crystal orbital methods, we elucidated candidates for monomer units with the high-spin ground states in the previous study of Part I [J. Chem. Phys. 113, 4035 (2000)] by employing density-functional (DFT) methods using Becke's and Becke's three parameter exchanges with Lee–Yang–Parr correlation or Hartree–Fock (HF) molecular orbital and post HF approximations. However, it was found that further computations applying other DFT functionals should be carried out to clarify the level of approximations which appropriately describe the electronic structures of magnetic molecules. In this part II, we present details of numerical results concerning magnetic properties and electronic structures for m-phenylene molecules with three neutral and one cation radicals by spin-polarized density functional methods using variety of local and nonlocal functionals and unrestricted molecular orbital methods including Møller–Plesset and coupled-cluster (CC) correlation corrections. The dependence of total, exchange and correlation energies, and spin densities on various approximated functionals is investigated thoroughly. The effective exchange integrals in the Heisenberg model are calculated by local and nonlocal DFT methods, and they are compared with those of complete active space (CAS) CI, CASSCF, and CASPT2. It is concluded that nonlocal DFT with density-gradient corrections can be used as a practical alternative to UCCSD(T) and CASPT2. The broken-symmetry Unrestricted Hartree–Fock (UHF) and DFT calculations of m-phenylene polyradicals with polar substituents are carried out to elucidate roles of superexchange interactions arising from the significant mixing of charge-transfer (CT) configurations. The resonance of covalent structures with CT or zwitterionic structures entails antiferromagnetic exchange interactions even in polyradicals with m-phenylene bridges; for example, substituted nitroxide polyradicals. Stable ferromagnetic polymers and dendrimers are designed on the basis of the theoretical grounds. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 2769-2780 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: We perform numerically exact calculations of quantum dynamics for a two-state molecular model system interacting with initially single-mode strongly amplitude- and strongly phase-squeezed fields (average photon number 〈n(circumflex)〉=8). The second-order correlation function for these fields are taken to be 2, which is equivalent to that for the chaotic field with the identical average photon number. Although the responses of the molecule for these two squeezed fields are relatively similar to those for the chaotic field as shown in a previous paper, there are found to be some significant differences among these fields in the dynamical behavior of quantum-phase distributions of photons, i.e., the Pegg–Barnett phase and the Q function distributions. These differences are also elucidated by the dynamics of the information entropy for the molecule, i.e., molecular entropy, which represents the degree of entanglement between the molecule and the photon field. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 111 (1999), S. 1309-1324 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Because it has been well-known that the effective exchange interaction of spins is much larger within a molecule than between molecules, it is very important to design high-spin polymers linking high-spin molecules with each other as a constituent unit to obtain molecule-based ferromagnetic materials with high transition temperature. Experimental efforts to synthesize such polymers extended in one- or two-dimensions have been made in recent years while theoretical treatment of infinite polymers has been behind in the sense that no study of electronic and magnetic structure calculations by ab initio periodic approaches exists until now. We examined the magnetic properties in m-phenylene and related molecules with organic radicals by density functional and molecular orbital methods as monomer units of high-spin polymers in Part I and Part II of this series, since it has already been confirmed experimentally and theoretically that m-phenylene coupling unit leads to the ferromagnetic coupling between spins. In Sec. III, we examine the possibility of ferromagnetic polymers in which organic radicals are arranged thorough m-phenylene bridge periodically in one dimension. For this purpose, ab initio crystal orbital methods based on density functional and Hartree–Fock approximations are employed for m-phenylene polymers with four species of C, CH, N, and NH+ radical groups as spin sources. It is shown that these polymers have the high-spin ground states and the density functional approaches can yield reasonable results which are comparable with the experiment. Implications of the calculated results are also discussed in relation to ferromagnetic polymers with different coupling units. © 1999 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 103 (1995), S. 4175-4191 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Various size-consistent approaches to the calculation of molecular hyperpolarizabilities are analyzed based on the double perturbation theory. General equations for the nth-order response property with respect to an external time-independent field are derived on the basis of the Rayleigh–Schrödinger perturbation theory (RSPT) and the coupled-cluster (CC) theory. The corresponding equations for the time-dependent case are also derived by the CC formalism, which is referred to as the time-dependent CC (TDCC) method. In order to clarify the spatial characteristics of polarizability and hyperpolarizability, we present an analysis method using a new concept "the polarizability and hyperpolarizability densities.'' As an application of the size-consistent methods, the static second hyperpolarizabilities (γ) of π-conjugated polymeric systems are calculated by the use of the uncoupled (UCHF), and coupled-Hartree–Fock (CHF) methods combined with the semiempirical INDO approximation. Characteristics of γ values calculated for regular polyenes, solitonlike polyenes and donor(D)–acceptor(A) disubstituted polyenes are investigated, particularly in relation to the chain-length effect. Further, we employ γ density analysis method, in which the third derivatives of the Mulliken charge densities against applied electric fields are plotted for exploring the local contributions of the constituent atoms to γ values. Results for the finite polyenes are also extrapolated to an infinity of the chain length to predict the intrinsic γ values per unit carbon–carbon (CC) bond of polymeric chains. Furthermore, the CHF+Møller–Plesset second-order perturbation (MP2) method in the PPP approximation is applied to polymeric systems with larger chain length in order to elucidate the electron correlation effects on the chain-length dependencies of γ values. © 1995 American Institute of Physics.
    Type of Medium: Electronic Resource
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