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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 116 (2002), S. 1892-1910 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: A detailed [C2H2NO+] potential-energy surface in singlet, including 48 minimum isomers and 73 transition states, is built up at the B3LYP/6-311G(d,p) and CCSD(T)/6-311G(2df,p) (single-point) levels in order to explore the mechanisms of the important ion–molecule reactions between CCN+/CNC+ and H2O and between HCO+/HOC+ and HCN/HNC. For the reactions of both CCN+ and CNC+ towards H2O, product HCO++HNC may be the most abundant followed by the much less HCO++HCN and then HCNH++CO. Significant discrepancies on the product distributions are found between our calculated results and two previous experimental findings. On the other hand, for the HCO++HCN/HNC reactions, the barrierless association may lead to the stable adducts OC(H)NCH+/OC(H)CNH+, while the proton-transfer may barrierlessly lead to product HCNH++CO via the hydrogen-bound complexes OC...HNCH+/OC...HCNH+. For the HOC++HCN/HNC reactions, both the barrierless proton-transfer and association-elimination processes can lead to HCNH++CO via the complexes CO...HNCH+/CO...HCNH+ and unstable adducts HOCNCH+/HOCCNH+, respectively. The computations reported in this paper may represent the first theoretical study on the chemical reactivity of the C2N+ ion, and may thus provide a useful guide for understanding the mechanisms of the other analogous reactions such as those of C2N+ with CH4, NH3, H2S and CH3OH, etc. The present calculations may also provide useful information for future laboratory investigations on the HCO+/HOC++HCN/HCN reactions that have not been previously studied. Interstellar implications of the title reactions are discussed. © 2002 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 10001-10006 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Molecular dynamics simulation starting from a lamellar crystal model of a single polyethylene chain is performed to investigate the lamellar reorganization during heating at the molecular level. It is shown that three stages are involved in the process of the reorganization: at temperatures 300 K〈T≤370 K the lamella thickens, in the region of 370 K〈T≤500 K the boundary premelting of the lamella occurs, and when T〉500 K the lamella starts to melt and becomes a random coil in the end. Particularly, the thickening process is investigated in our simulations. It is found that the lamellar thickening occurs in discrete steps and is driven mainly by the van der Waal attraction between the chain segments. There are two mechanisms for the lamellar thickening. At lower temperature the thickening occurs by the sliding diffusion of adjacent chain segments, while at higher temperature the recrystallization after the partial melting of thinner stems leads to the thickening. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 115 (2001), S. 3916-3922 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: By means of molecular dynamics simulation, the crystallization process of the copolymer (ethylene-co-propene) with different branch distributions is studied at the molecular level. It is shown that subglobules formed at the branch sites along the copolymer chains and subsequently coalesced into a single globule and then developed to a lamellar structure in the end. This process can be considered as crystal nucleation and growth at the early stage of the copolymer crystallization. In the nucleation the branch acts as a nucleating seed and in the crystal growth the branch is rejected from the crystal region as a defect. The driving force for the relaxation process is the attractive van der Waals interaction between the chain segments. Furthermore, it is found that the branch distribution is an important factor in determining the crystallinity of the copolymer, when the comonomer composition and the molecular weight of the copolymers are fixed, as a blocky type of copolymer will show nearly unhampered crystallization and a true random copolymer will show a hindered one. © 2001 American Institute of Physics.
    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 114 (2001), S. 5170-5179 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The potential-energy surface of the interstellar molecule C4N is explored at the B3LYP/6-311G(d) level of theory. Thirteen isomers including the linear, three-membered ring, four-membered ring, A-like, Y-like, and cage-like structures are located as minima connected by 23 interconversion transition states. The structures of the most relevant isomers and transition states are further optimized at the QCISD/6-311G(d) level followed by single-point energy calculations at the MP4SDTQ, CCSD(T), and QCISD(T) levels with the 6-311G(2df) basis set. At the CCSD(T)/6-311G(2df)//QCISD/6-311G(d) level, the lowest-lying isomer is a linear structure CCCCN 1 followed by a CCC three-membered ring structure 4 with exocyclic CCN bonding that lies only 2.8 kcal/mol higher. The third and fourth low-lying isomers possess a CCC three-membered ring structure 5 with exocyclic CNC bonding at 21.4 kcal/mol and a linear structure CCCNC 2 at 23.4 kcal/mol, respectively. All the four isomers 1, 2, 4, and 5 and another high-lying isomer 3 with a linear CCNCC structure at 62.5 kcal/mol are shown to have considerable kinetic stability towards isomerization and dissociation. Thus, all the five isomers may be experimentally observable. Possible formation of these five stable C4N isomers in interstellar space is discussed. Finally, our calculations show that the Møller–Plesset methods fail to predict even qualitatively the energetic properties between the four low-lying isomers 1, 2, 4, and 5, in comparison with the QCISD and CCSD results. This paper indicates that C4N may be the first interstellar molecule with stable low-lying cyclic isomers among the CnN radical series to be detectable in near future. The results presented in this paper may provide useful information for future laboratory and interstellar identification of various C4N isomers. © 2001 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 113 (2000), S. 1745-1754 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dissociation and isomerization stability of the linear cyanogen isomer CCNN, a formally charge-transfer species comprising C2− and N2+, is theoretically investigated by means of ab initio methods, including the Hartree–Fock (HF), the Møller–Plesset perturbation theory from second through fourth order (MP2, MP4SDQ, MP4SDTQ), the configuration interaction with singles and doubles (CISD), the quadratic configuration interaction with singles and doubles (QCISD) as well as with triples [QCISD(T)], and the density functional theory (DFT) including Beck's three parameter hybrid methods with the Lee–Yang–Parr correlation functional (B3LYP) and with the Perdew–Wang 91 correlation functional (B3PW91) methods. At the QCISD(T)/6-311G(3df)//QCISD(T)/6-311G(d) level with QCISD/6-311G(d) zero-point vibrational energy (ZPVE) correction, the barriers from CCNN to the NNC three-membered ring structure with exocyclic C–C bonding and to the dissociation products C2 and N2 are predicted to be 42.1 and 51.8 kcal/mol, respectively. The QCISD(T)/6-311G(3df) potential energy surface of C2N2 indicates that CCNN may be kinetically more stable than the other two well-studied isomers CNCN and CNNC. Thus, although CCNN is thermodynamically less favorable due to its high energy, it is still experimentally observable. Moreover, a barrier of 5.5 kcal/mol is predicted for the reverse association reaction between C2 and N2 to produce CCNN at the QCISD(T)/6-311G(3df)//QCISD(T)/6-311G(d)+ZPVE level, while both B3LYP and B3PW91 methods erroneously predict a barrierless association process. Finally, the possible strategy for the formation of CCNN in laboratory and in interstellar space is discussed in detail. The calculated results may provide a useful guide for future laboratory and interstellar identification of the last kinetically stable isomer of cyanogen, CCNN. © 2000 American Institute of Physics.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 87 (1983), S. 3412-3414 
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Journal of mathematical chemistry 21 (1997), S. 159-182 
    ISSN: 1572-8897
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mathematics
    Notes: Abstract The construction of a symplectic basis set with 〉N electrons is exhibited by means of three kinds of units, the first kind geminal, the second kind geminal and the one‐particle operators. The optimization procedure of the variation method is extended to the coefficients in the linear sum of the symplectic bases, the parameters in the geminals, and the orbitals. For practical use, these bases are expanded explicitly as a linear sum of the Slater determinants. For illustration, the LiH molecule, which is taken as an example, is calculated by using some symplectic bases.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 1209-1220 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Two small groups (E, σν) and (E, C2) are proposed to describe the orbital symmmetry of the whole reaction paths with respect to suprafacial and antarafacial sigmatropic rearrangements. Furthermore, the symmetries of the two small groups are extended to the systems as a many body treatment performed by Matsen.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 22 (1982), S. 665-679 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The groups with local symmetries are employed to explore the intrinsic symmetries of various kinds of cycloadditions to become apparent ones. For the electrocyclic reactions, the concept of local symmetry can still be applied equivalently, but no new result can be achieved. Furthermore, the local symmetries are generalized to the systems as a many body treatment performed by Matsen.
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 25 (1984), S. 1045-1054 
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The unitarily invariant decomposition of Hermitian operators for a boson system is performed by means of the symmetry of group SO(2, 1) and the decomposition is also closely related with Lie algebra.
    Type of Medium: Electronic Resource
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