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  • Articles: DFG German National Licenses  (58)
  • 2015-2019
  • 2000-2004  (58)
  • Chemistry and Pharmacology  (58)
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  • 1
    ISSN: 0066-426X
    Source: Annual Reviews Electronic Back Volume Collection 1932-2001ff
    Topics: Chemistry and Pharmacology , Physics
    Notes: Abstract Proteins directly control the nucleation and growth of biominerals, but the details of molecular recognition at the protein-biomineral interface remain poorly understood. The elucidation of recognition mechanisms at this interface may provide design principles for advanced materials development in medical and ceramic composites technologies. Here, we describe both the theory and practice of double-quantum solid-state NMR (ssNMR) structure-determination techniques, as they are used to determine the secondary structures of surface-adsorbed peptides and proteins. In particular, we have used ssNMR dipolar techniques to provide the first high-resolution structural and dynamic characterization of a hydrated biomineralization protein, salivary statherin, adsorbed to its biologically relevant hydroxyapatite (HAP) surface. Here, we also review NMR data on peptides designed to adsorb from aqueous solutions onto highly porous hydrophobic surfaces with specific helical secondary structures. The adsorption or covalent attachment of biological macromolecules onto polymer materials to improve their biocompatibility has been pursued using a variety of approaches, but key to understanding their efficacy is the verification of the structure and dynamics of the immobilized biomolecules using double-quantum ssNMR spectroscopy.
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 112 (2000), S. 6355-6364 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The ring-collapse mechanism that suggests the reactions among the mono- to polycyclic carbon clusters has been analyzed using semiempirical AM1 and HF/6-31G* methods. The two cage structures D2 (chiral) and Td (achiral) for the C28 clusters are considered. Basing on the ring-stacking/circumscribing model and the ring-collapse mechanism various precursors are selected along with some appropriate carbon belts. Reactions between the precursors and the belts are found to be endoergic and lead to stable intermediates. All these stacking processes follow gradual and sequential paths. Various possible transition states structures (TSs) have been located and the barrier heights are found to be well within the earlier prescribed limits. Further, stacking the stable intermediates by suitable carbon belts generate the desired cage structures. The second step of the stacking resembles the annealing mechanism for the formation of the cage structures that is essentially an exoergic process. In this annealing process cascade-type bond formation is visualized. Finally, basing on the deformation energies of the precursors and the barrier heights, it is observed that monocyclic precursors are more suitable for the fullerene growth mechanism. © 2000 American Institute of Physics.
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  • 3
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: By using a step-scan Fourier transform spectrometer, we have studied collisionally-induced rotational energy transfer (RET) of the CH A(2Δ) (N≤16,v=0) and B(2Σ−) (N≤16,v=0) states. The collision partners used for the B state are He, Ar, N2, CO, N2O, and CHBr3, while He and Ar are for the A state. The time-resolved spectra obtained in the nanosecond regime may yield the RET information straightforward under a single pressure of the collider. The resultant RET rate constants for both states range from 10−12 to 10−10 cm3 molecule−1 s−1, comparable to the gas kinetic. The trend follows the order of He∼Ar〈N2∼CO〈N2O〈CHBr3 for the B state, and He〈Ar for the A state. For the B state, the findings of multi-quantum changing collisions up to ΔN=±3 and markedly large rate constants imply that the RET collisions are dominated by long-range attractive force. The collision complexes possibly formed between the CH(B) and the colliders are long-lived enough to allow for effective removal of the rotational energy more than a quantum level in a single collision. In contrast, a single quantum change in the RET collision found in the A state suggests dominance of a repulsive interaction between the colliding species, which has been verified previously in the measurements of temperature dependence of the electronic quenching. © 2000 American Institute of Physics.
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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. 10548-10556 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Ab initio static and dynamic (hyper)polarizability calculations at the time-dependent coupled-perturbed Hartree–Fock level have been carried out on polyyne, all-trans polyacetylene (PA), and trans-transoïd polymethineimine by a noniterative method. The dependence on basis set and on the number of neighboring unit cells exactly included has been investigated. The 6-31G basis set with nine neighboring unit cells, and long-range Coulomb interactions taken into account, was utilized in the final calculations. Although in many instances our results are the first that have been obtained we compare with oligomer calculations wherever possible. For PA the theoretical result is also compared with experiment and the main reasons for the existing discrepancy are addressed. © 2001 American Institute of Physics.
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  • 5
    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.
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 114 (2001), S. 7633-7643 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Previously we have shown how to obtain the electric properties of a polymer or other periodic system at the coupled Hartree–Fock level by direct, analytical calculation rather than by extrapolation of oligomer results. Here we add computationally simpler noniterative formulas and test the methodology for the longitudinal dipole moment (μ), polarizability (α), first hyperpolarizability (β), and second hyperpolarizability (γ) of five quasilinear polymers: (LiH)n, (FH)n, (H2O)n, trans-polymethineimine (–CNH–)n, and trans-polyacetylene (–CH=CH–)n. The polymer values are in good agreement with large-oligomer calculations. In this connection the role of phase factors, particularly in determining the dipole moment, is elucidated. We are now in a good position to include electron correlation using methods analogous to those employed for molecular systems. © 2001 American Institute of Physics.
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  • 7
    Electronic Resource
    Electronic Resource
    Bingley : Emerald
    Pigment & resin technology 33 (2004), S. 280-286 
    ISSN: 0369-9420
    Source: Emerald Fulltext Archive Database 1994-2005
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: UV curing technology has a number of unique advantages over the conventional curing technologies. However, until very recently, there had been few successful examples of the application of UV curing technology in ink-jet printing. Several reasons, including the requirement of low viscosity for ink-jet printing inks, were responsible for the lack of development of UV curable ink-jet printing inks. This paper describes, in some details, the challenges that a formulator had to face in developing UV curable ink-jet printing inks, together with information on the status quo of UV curable ink-jet printing technology.
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  • 8
    ISSN: 1600-5740
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: Seven Group 1 and Group 2 1,5-naphthalenedisulfonates (1,5-nds) have been synthesized and structurally characterized by single-crystal X-ray diffraction, IR spectroscopy and thermal gravimetric analysis. For Group 1 metal complexes, with M = Li+ (1), Na+ (2) and K+ (3), all crystallize in the same space group (P21/c) with the same composition, [M2(1,5-nds)(H2O)2]. They adopt similar three-dimensional packing arrangements with the metal–sulfonate inorganic layers pillared by naphthalene rings. However, the coordination behavior of three metal cations toward the SO_3^- group and water molecule are different, resulting in different architectures for the inorganic portion. For Group 2 complexes with M = Mg2+ (4), Ca2+ (5), Sr2+ (6) and Ba2+ (7), Mg2+ shows no direct coordination by the SO_3^- group while Ca2+ is coordinated by four SO_3^- groups and a two-dimensional network is formed. Complexes (6) and (7) are isostructural, adopting the same three-dimensional, inorganic–organic pillared framework as seen for (1)–(3). The coordination behavior of the metal cations in these structures neatly illustrates the increase in coordination strength with decreasing charge/radius ratio for Group 1 and Group 2 metal cations with large organic anions.
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 56 (2000), S. e181-e182 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: In the title molecular complex, (I), the W atom is in an octahedral environment with four equatorial carbonyl ligands and a fifth in an axial position trans to the monodentate dipyridylamine ligand. The long dimension of this last bisects the angle between two of the equatorial carbonyl groups and while the non-bonded pyridyl N atom is directed away from the W atom, the bridging amine group is directed towards it. Thus, in addition to the N atom to which it is attached, the amino H has two nearest neighbour C atoms of equatorial carbonyl groups but does not participate in hydrogen bonding in any real or usual sense. The W—C bond distance for the axial carbonyl group is notably less than those of the equatorial groups.
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  • 10
    Electronic Resource
    Electronic Resource
    Oxford [u.a.] : International Union of Crystallography (IUCr)
    Acta crystallographica 57 (2001), S. 1168-1170 
    ISSN: 1600-5759
    Source: Crystallography Journals Online : IUCR Backfile Archive 1948-2001
    Topics: Chemistry and Pharmacology , Geosciences , Physics
    Notes: The title mixed-metal compound, [Cu(C2H8N2)2(H2O)2][Ni(C2H8N2)3]2(C10H6O6S2)3·4H2O, was obtained during investigations of the porous frameworks constructed by amino-coordinated metal complex cations and large organic anions. All three naphthalene-2,6-disulfonate anions and the [Cu(en)2(H2O)2]2+ cation are located on crystallographic inversion centers and assemble into an extended two-dimensional network through intermolecular hydrogen bonds, creating cavities in which the [Ni(en)3]2+ cations and water molecules are included.
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