1,107 research outputs found

    Correlation of structural and spectroscopic properties of a photosynthetic reaction center

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    Polarized spectra of absorption and light-induced absorbance changes are presented for the crystallized reaction centers of Rhodopseudomonas viridis. We find that a model based on extended dipole interaction between all six pigments is capable of interpreting detailed features such as the contributions from the individual pigments to the various absorption peaks. Even though the pigments are arranged in approximate C2 symmetry, the optical spectra together with the calculations reflect deviations from this symmetry, which may be important in understanding the electron pathway

    Stimulation of Adenosine A 3 Receptors in Cerebral Ischemia: Neuronal Death, Recovery, or Both?

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    The role of the adenosine A 3 receptor continues to baffle, and, despite an increasing number of studies, the currently available data add to, rather than alleviate, the existing confusion. The reported effects of adenosine A 3 receptor stimulation appear to depend on the pattern of drug administration (acute vs. chronic), dose, and type of the target tissue. Thus, while acute exposure to A 3 receptor agonists protects against myocardial ischemia, it is severely damaging when these agents are given shortly prior to cerebral ischemia. Mast cells degranulate when their A 3 receptors are stimulated. Degranulation of neutrophils is, on the other hand, impaired. While reduced production of reactive nitrogen species has been reported following activation of A 3 receptors in collagen-induced arthritis, the process appears to be enhanced in cerebral ischemia. Indeed, immunocytochemical studies indicate that both pre- and postischemic treatment with A 3 receptor antagonist dramatically reduces nitric oxide synthase in the affected hippocampus. Even more surprisingly, low doses of A 3 receptor agonists seem to enhance astrocyte proliferation, while high doses induce their apoptosis. This review concentrates on the studies of cerebral A 3 receptors and, based on the available evidence, discusses the possibility of adenosine A 3 receptor serving as an integral element of the endogenous cerebral neuroprotective complex consisting of adenosine and its receptors.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/75391/1/j.1749-6632.1999.tb07984.x.pd

    14N and 15N coupling constants of the oxidized primary donor P-860 of bacterial photosynthesis obtained by electron spin echo envelope modulation spectroscopy

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    An electron spin echo modulation frequency analysis of P+-860 is performed in 14N chromatophores of Rhodospirillum rubrum, and in 15N substituted reaction centers from Rhodopseudomonas sphaeroides 2.4.1. For the 14N material two sets of nuclear quadrupole parameters are obtained. From the frequencies found for 15N reaction centers the perpendicular, parallel and isotropic hyperfine previous termcouplingnext term constants of three of the four bacteriochlorophyll nitrogen nuclei are inferred

    0105 v.2 Probing the Surrounding of a Cobalt(II) Porphyrin and its Superoxo Complex by EPR Techniques

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    Abstract. Octaethylporphyrinato-cobalt(II), Co(II)OEP, was studied by electron paramagnetic resonance (EPR) and electron-nuclear double resonance (ENDOR) in frozen solutions of methanol, tetrahydrofuran and pyridine diluted into chloroform. Oxygenation led to the respective paramagnetic superoxo complexes Co(III)OEPpyO 2 # . The EPR spectra demonstrate strong differences in the axial ligation states ((base-on)/(base-off)) and ease of the oxygenation process. Additional ENDOR studies with partial orientation selection along the principal g tensor axes are performed for resolution of the 1 H, 14/15 N and 59 Co hyperfine (hf) coupling constants. This allows a comparison of the electron spin density distribution of the superoxo complex and its precursor. The data are interpreted in the framework of a more rigorous and detailed theoretical configuration interaction model than previously presented in the literature. The theoretical treatment shows that the structure of the superoxo complex is best described in a three-orbital model with contributions from the cobalt 3d, 4s, and oxygen p orbitals. The analysis reproduces the experimental g and Co hf data yielding the relative energies of the MOs and the MO coefficients for the description of the spin density distribution in the Co(II) complex and its superoxo complex. To demonstrate the generality of the approach and possible applications, a comparison is made with the vitamin B 12r system. Furthermore, it provides detailed insight into the electronic and geometric changes resulting from axial ligation and oxygenation of the Co(II)OEP complex; this information can be used for predictions of the catalytic activity

    Structured near-infrared Magnetic Circular Dichroism spectra of the Mn₄CaO₅ cluster of PSII in T. vulcanus are dominated by Mn(IV) d-d 'spin-flip' transitions

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    Photosystem II passes through four metastable S-states in catalysing light-driven water oxidation. Variable temperature variable field (VTVH) Magnetic Circular Dichroism (MCD) spectra in PSII of Thermosynochococcus (T.) vulcanus for each S-state are reported. These spectra, along with assignments, provide a new window into the electronic and magnetic structure of Mn₄CaO₅. VTVH MCD spectra taken in the S₂state provide a clear g=2, S=1/2 paramagnetic characteristic, which is entirely consistent with that known by EPR. The three features, seen as positive (+) at 749nm, negative (-) at 773nm and (+) at 808nm are assigned as ⁴A→²E spin-flips within the d³ configuration of the Mn(IV) centres present. This assignment is supported by comparison(s) to spin-flips seen in a range of Mn(IV) materials. S₃ exhibits a more intense (-) MCD peak at 764nm and has a stronger MCD saturation characteristic. This S₃ MCD saturation behaviour can be accurately modelled using parameters taken directly from analyses of EPR spectra. We see no evidence for Mn(III) d-d absorption in the near-IR of any S-state. We suggest that Mn(IV)-based absorption may be responsible for the well-known near-IR induced changes induced in S₂ EPR spectra of T. vulcanus and not Mn(III)-based, as has been commonly assumed. Through an analysis of the nephelauxetic effect, the excitation energy of S-state dependent spin-flips seen may help identify coordination characteristics and changes at each Mn(IV). A prospectus as to what more detailed S-state dependent MCD studies promise to achieve is outlined.We recognise the support of the Australian Research Council through grants DP110104565 and DP150103137 (E.K.), FT140100834 (N.C) and MEXT/JSPS of Japan through a Grant-in-Aid for Specially Promoted Research No. 24000018 (J.R.S.)

    Integration of Catalysis with Storage for the Design of Multi-Electron Photochemistry Devices for Solar Fuel

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    Decarbonization of the transport system and a transition to a new diversified energy system that is scalable and sustainable, requires a widespread implementation of carbon-neutral fuels. In biomimetic supramolecular nanoreactors for solar-to-fuel conversion, water-splitting catalysts can be coupled to photochemical units to form complex electrochemical nanostructures, based on a systems integration approach and guided by magnetic resonance knowledge of the operating principles of biological photosynthesis, to bridge between long-distance energy transfer on the short time scale of fluorescence, ~10−9 s, and short-distance proton-coupled electron transfer and storage on the much longer time scale of catalysis, ~10−3 s. A modular approach allows for the design of nanostructured optimized topologies with a tunneling bridge for the integration of storage with catalysis and optimization of proton chemical potentials, to mimic proton-coupled electron transfer processes in photosystem II and hydrogenase

    School census autumn 2017 : 16 to 19 reports : user guide

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    The synthesis of a series of cobalt NHC complexes of the types [Co­(NHC)<sub>2</sub>(CO)­(NO)] (NHC = <i>i</i>Pr<sub>2</sub>Im (<b>2</b>), <i>n</i>Pr<sub>2</sub>Im (<b>3</b>), Cy<sub>2</sub>Im (<b>4</b>), Me<sub>2</sub>Im (<b>5</b>), <i>i</i>Pr<sub>2</sub>ImMe (<b>6</b>), Me<sub>2</sub>ImMe (<b>7</b>), Me<i>i</i>PrIm (<b>8</b>), Me<i>t</i>BuIm (<b>9</b>); R<sub>2</sub>Im = 1,3-dialkylimidazolin-2-ylidene) and [Co­(NHC)­(CO)<sub>2</sub>(NO)] (NHC = <i>i</i>Pr<sub>2</sub>Im (<b>13</b>), <i>n</i>Pr<sub>2</sub>Im (<b>14</b>), Me<sub>2</sub>Im (<b>15</b>), <i>i</i>Pr<sub>2</sub>ImMe (<b>16</b>), Me<sub>2</sub>ImMe (<b>17</b>), Me<i>i</i>PrIm (<b>18</b>), Me<i>t</i>BuIm (<b>19</b>)) from the reaction of the NHC with [Co­(CO)<sub>3</sub>(NO)] (<b>1</b>) is reported. These complexes have been characterized using elemental analysis, IR spectroscopy, multinuclear NMR spectroscopy, and in many cases by X-ray crystallography. Bulky NHCs tend to form the mono-NHC-substituted complexes [Co­(NHC)­(CO)<sub>2</sub>(NO)], even from the reaction with an stoichiometric excess of the NHC, as demonstrated by the synthesis of [Co­(Dipp<sub>2</sub>Im)­(CO)<sub>2</sub>(NO)] (<b>11</b>), [Co­(Mes<sub>2</sub>Im)­(CO)<sub>2</sub>(NO)] (<b>12</b>), and [Co­(<sup>Me</sup>cAAC)­(CO)<sub>2</sub>(NO)] (<b>20</b>). For <i>t</i>Bu<sub>2</sub>Im a preferred coordination via the NHC backbone (“abnormal” coordination at the 4-position) was observed and the complex [Co­(<i>t</i>Bu<sub>2</sub><sup>a</sup>Im)­(CO)<sub>2</sub>(NO)] (<b>10</b>) was isolated. All of these complexes are volatile, are stable upon sublimation and prolonged storage in the gas phase, and readily decompose at higher temperatures. Furthermore, DTA/TG analyses revealed that the complexes [Co­(NHC)<sub>2</sub>(CO)­(NO)] are seemingly more stable toward thermal decomposition in comparison to the complexes [Co­(NHC)­(CO)<sub>2</sub>(NO)]. We thus conclude that the cobalt complexes of the type [Co­(NHC)­(CO)<sub>2</sub>(NO)] and [Co­(NHC)<sub>2</sub>(CO)­(NO)] have potential for application as precursors in the vapor deposition of thin cobalt films

    Optical and Infrared Spectroscopy

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    Contains research objectives and reports on one research project
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