-
3
-
-
0034423026
-
Primary processes in photosynthesis: What do we learn from high-field EPR spectroscopy?
-
Mobius K.Primary processes in photosynthesis: what do we learn from high-field EPR spectroscopy? Chem Soc Rev 29 2000 129-139
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(2000)
Chem Soc Rev
, vol.29
, pp. 129-139
-
-
Mobius, K.1
-
4
-
-
0001743149
-
A high-field/high-frequency heterodyne induction-mode electron paramagnetic resonance spectrometer operating at 360 GHz
-
Fuchs M.R.Prisner T.F.Mobius K.A high-field/high-frequency heterodyne induction-mode electron paramagnetic resonance spectrometer operating at 360 GHz Rev Sci Instrum 70 1999 3681-3683
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Rev Sci Instrum
, vol.70
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-
-
Fuchs, M.R.1
Prisner, T.F.2
Mobius, K.3
-
5
-
-
0035528076
-
Single-crystal EPR studies of transition-metal ions in inorganic crystals at very high frequency
-
Misra S.K.Andronenko S.I.Earle K.A.Freed J.H.Single-crystal EPR studies of transition-metal ions in inorganic crystals at very high frequency Appl Magn Reson 21 2001 549-561
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Appl Magn Reson
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Misra, S.K.1
Andronenko, S.I.2
Earle, K.A.3
Freed, J.H.4
-
6
-
-
0035528059
-
High-Field/High-Frequency EPR spectrometer operating in pulsed and continuous-wave mode at 180 GHz
-
1/2) is achieved. Microwave π/2 pulse lengths down to 60 ns are possible. The absolute sensitivity in pulse experiments is 40 times better than at X-band, which is crucial for samples that exist only in tiny amounts or with a limited size
-
1/2) is achieved. Microwave π/2 pulse lengths down to 60 ns are possible. The absolute sensitivity in pulse experiments is 40 times better than at X-band, which is crucial for samples that exist only in tiny amounts or with a limited size.
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(2001)
Appl Magn Reson
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, pp. 257-274
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Rohrer, M.1
Brugmann, O.2
Kinzer, B.3
Prisner, T.F.4
-
7
-
-
18444398666
-
How and why the characterization of magnetic materials can give directions in the methodological development in high field-high frequency EPR
-
Brunel L.C.Caneschi A.Dei A.Friselli D.Gatteschi D.Hassan A.K.Lenci L.Martinelli M.Massa C.A.Pardi L.A.Popescu F.Ricci I.Sorace L.How and why the characterization of magnetic materials can give directions in the methodological development in high field-high frequency EPR Res Chem Intermed 28 2002 215-229
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Res Chem Intermed
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Brunel, L.C.1
Caneschi, A.2
Dei, A.3
Friselli, D.4
Gatteschi, D.5
Hassan, A.K.6
Lenci, L.7
Martinelli, M.8
Massa, C.A.9
Pardi, L.A.10
Popescu, F.11
Ricci, I.12
Sorace, L.13
-
10
-
-
0000858387
-
Magnetic-field-induced orientation of photosynthetic reaction centres as revealed by time-resolved W-band EPR of spin-correlated radical pairs
-
Berthold T.Bechtold M.Heinen U.Link G.Poluektov O.Utschig L.Tang J.Thurnauer M.C.Kothe G.Magnetic-field-induced orientation of photosynthetic reaction centres as revealed by time-resolved W-band EPR of spin-correlated radical pairs J Phys Chem B 103 1999 10733-10736
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J Phys Chem B
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Berthold, T.1
Bechtold, M.2
Heinen, U.3
Link, G.4
Poluektov, O.5
Utschig, L.6
Tang, J.7
Thurnauer, M.C.8
Kothe, G.9
-
11
-
-
0037178941
-
EPR spectra from 'EPR-silent' species: High-frequency and high-field EPR spectroscopy of pseudotetrahedral complexes of nickel(II)
-
-1 in integer spin systems, represented here by Ni(II) complexes (S=1)
-
-1 in integer spin systems, represented here by Ni(II) complexes (S=1).
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(2002)
Inorg Chem
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-
Krzystek, J.1
Park, J.H.2
Meisel, M.W.3
Hitchman, M.A.4
Stratemeier, H.5
Brunel, L.C.6
Telser, J.7
-
13
-
-
0037089345
-
4-doped polyaniline
-
This study shows how saturation and passage effects, which are often encountered in high-field EPR, can be put to good use in deriving relaxation times. The relaxation data in turn provide insight into the dynamics of the spin carriers, which can then be compared to the dynamics of the charge carriers
-
4-doped polyaniline Phys Rev B 65 2002 155205 This study shows how saturation and passage effects, which are often encountered in high-field EPR, can be put to good use in deriving relaxation times. The relaxation data in turn provide insight into the dynamics of the spin carriers, which can then be compared to the dynamics of the charge carriers.
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(2002)
Phys Rev B
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Krinichnyi, V.I.1
Roth, H.K.2
Hinrichsen, G.3
Lux, F.4
Lüders, K.5
-
15
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-
0000907326
-
Electron nuclear double resonance of metalloenzymes
-
Hoffman B.M.Electron nuclear double resonance of metalloenzymes Acc Chem Res 24 1991 164-170
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(1991)
Acc Chem Res
, vol.24
, pp. 164-170
-
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Hoffman, B.M.1
-
17
-
-
0037045479
-
EPR studies on film formation of colloidal dispersions: 1. Site selectivity and techniques
-
Cramer S.E.Jeschke G.Spiess H.W.EPR studies on film formation of colloidal dispersions: 1. Site selectivity and techniques Macromol Chem Phys 203 2002 182-191
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(2002)
Macromol Chem Phys
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Cramer, S.E.1
Jeschke, G.2
Spiess, H.W.3
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18
-
-
36849115846
-
Ligand ENDOR of metal complexes in powders
-
Rist G.H.Hyde J.S.Ligand ENDOR of metal complexes in powders J Chem Phys 52 1970 4633-4643
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(1970)
J Chem Phys
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Rist, G.H.1
Hyde, J.S.2
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19
-
-
48549111357
-
General theory of polycrystalline ENDOR patterns-g and hyperfine tensors of arbitrary symmetry and relative orientation
-
Hoffman B.M.Martinsen J.Venters R.A.General theory of polycrystalline ENDOR patterns-g and hyperfine tensors of arbitrary symmetry and relative orientation J Magn Reson 59 1984 110-123
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(1984)
J Magn Reson
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Hoffman, B.M.1
Martinsen, J.2
Venters, R.A.3
-
20
-
-
0034810091
-
40 as studied by hyperfine sublevel correlation spectroscopy and pulsed electron nuclear double resonance at W- and X-band frequencies
-
Both the vanadium-phosphorous distance of 0.42 nm and the orientation of the vanadium-phosphorous vector with respect to the vanadium oxygen bond could be determined by using high-field ENDOR. Several existing models for the structure of the catalytically active heteropolyanion could thus be excluded
-
40 as studied by hyperfine sublevel correlation spectroscopy and pulsed electron nuclear double resonance at W- and X-band frequencies J Am Chem Soc 123 2001 4577-4584 Both the vanadium-phosphorous distance of 0.42 nm and the orientation of the vanadium-phosphorous vector with respect to the vanadium oxygen bond could be determined by using high-field ENDOR. Several existing models for the structure of the catalytically active heteropolyanion could thus be excluded.
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(2001)
J Am Chem Soc
, vol.123
, pp. 4577-4584
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-
Poppl, A.1
Manikandan, P.2
Kohler, K.3
Maas, P.4
Strauch, P.5
Bottcher, R.6
Goldfarb, D.7
-
21
-
-
0037198704
-
Interactions of Cu(II) ions with framework Al in high Si: Al zeolite Y as determined from X- and W-band pulsed EPR/ENDOR spectroscopies
-
Carl P.J.Vaughan D.E.W.Goldfarb D.Interactions of Cu(II) ions with framework Al in high Si:Al zeolite Y as determined from X- and W-band pulsed EPR/ENDOR spectroscopies J Phys Chem B 106 2002 5428-5437
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J Phys Chem B
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Carl, P.J.1
Vaughan, D.E.W.2
Goldfarb, D.3
-
22
-
-
0036695246
-
Self-trapped hole in silver chloride crystals: A pulsed EPR/ENDOR study at 95 GHz
-
A detailed picture of spin density distribution of the self-trapped hole could be derived from single-crystal ENDOR measurements at W-band frequencies and could be interpreted by a 'bare' Jahn-Teller distortion without involvement of a nearby vacancy or impurity
-
Bennebroek M.T.van Duijn-Arnold A.Schmidt J.Poluektov O.G.Baranov P.G.Self-trapped hole in silver chloride crystals: a pulsed EPR/ENDOR study at 95 GHz Phys Rev B 66 2002 054305 A detailed picture of spin density distribution of the self-trapped hole could be derived from single-crystal ENDOR measurements at W-band frequencies and could be interpreted by a 'bare' Jahn-Teller distortion without involvement of a nearby vacancy or impurity.
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Phys Rev B
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-
Bennebroek, M.T.1
van Duijn-Arnold, A.2
Schmidt, J.3
Poluektov, O.G.4
Baranov, P.G.5
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23
-
-
0000427269
-
Pulsed ENDOR spectroscopy at large thermal spin polarizations and the absolute sign of the hyperfine interaction
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Bennebroek M.T.Schmidt J.Pulsed ENDOR spectroscopy at large thermal spin polarizations and the absolute sign of the hyperfine interaction J Magn Reson 128 1997 199-206
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(1997)
J Magn Reson
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Bennebroek, M.T.1
Schmidt, J.2
-
24
-
-
0035743911
-
The effect of spin relaxation on ENDOR spectra recorded at high magnetic fields and low temperatures
-
Epel B.Poppl A.Manikandan P.Vega S.Goldfarb D.The effect of spin relaxation on ENDOR spectra recorded at high magnetic fields and low temperatures J Magn Reson 148 2001 388-397
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(2001)
J Magn Reson
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Epel, B.1
Poppl, A.2
Manikandan, P.3
Vega, S.4
Goldfarb, D.5
-
25
-
-
0035528061
-
High-field ENDOR and the sign of the hyperfine coupling
-
A nice overview of all the known asymmetries in high-field ENDOR spectra associated with thermal polarization at low temperatures
-
Epel B.Manikandan P.Kroneck P.M.H.Goldfarb D.High-field ENDOR and the sign of the hyperfine coupling Appl Magn Reson 21 2001 287-297 A nice overview of all the known asymmetries in high-field ENDOR spectra associated with thermal polarization at low temperatures.
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(2001)
Appl Magn Reson
, vol.21
, pp. 287-297
-
-
Epel, B.1
Manikandan, P.2
Kroneck, P.M.H.3
Goldfarb, D.4
-
26
-
-
0000294079
-
A critical validation of density functional and coupled-cluster approaches for the calculation of EPR hyperfine coupling constants in transition metal complexes
-
Central ion hyperfine couplings in transition metal complexes that are computed with current approaches should be interpreted with much caution
-
Munzarová M.Kaupp M.A critical validation of density functional and coupled-cluster approaches for the calculation of EPR hyperfine coupling constants in transition metal complexes J Phys Chem A 103 1999 9966-9983 Central ion hyperfine couplings in transition metal complexes that are computed with current approaches should be interpreted with much caution.
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(1999)
J Phys Chem A
, vol.103
, pp. 9966-9983
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-
Munzarová, M.1
Kaupp, M.2
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27
-
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0001644326
-
Calculations of isotropic hyperfine coupling constants of organic radicals. An evaluation of semiempirical, Hartree-Fock, and density functional methods
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Batra R.Giese B.Spichty M.Gescheidt G.Houk K.N.Calculations of isotropic hyperfine coupling constants of organic radicals. An evaluation of semiempirical, Hartree-Fock, and density functional methods J Phys Chem 100 1996 18371-18379
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J Phys Chem
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, pp. 18371-18379
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Batra, R.1
Giese, B.2
Spichty, M.3
Gescheidt, G.4
Houk, K.N.5
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28
-
-
0036525727
-
Quantum chemical calculations of [NiFe] hydrogenase
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Stein M.Lubitz W.Quantum chemical calculations of [NiFe] hydrogenase Curr Opin Chem Biol 6 2002 243-249 This overview shows that in favorable cases DFT computations of EPR parameters can be extremely useful for understanding the electronic structure of paramagnetic intermediates in catalytic reaction pathways.
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(2002)
Curr Opin Chem Biol
, vol.6
, pp. 243-249
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-
Stein, M.1
Lubitz, W.2
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29
-
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0037076050
-
A pulse EPR and ENDOR investigation of the electronic structure of a sigma-carbon-bonded cobalt(IV) corrole
-
Harmer J.Van Doorslaer S.Gromov I.Broring M.Jeschke G.Schweiger A.A pulse EPR and ENDOR investigation of the electronic structure of a sigma-carbon-bonded cobalt(IV) corrole J Phys Chem B 106 2002 2801-2811
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(2002)
J Phys Chem B
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Harmer, J.1
Van Doorslaer, S.2
Gromov, I.3
Broring, M.4
Jeschke, G.5
Schweiger, A.6
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31
-
-
0037139510
-
Density functional calculations of electronic g-tensors for semiquinone radical anions. The role of hydrogen bonding and substituent effects
-
This study shows that substituent effects on semiquinones are quantitatively predicted by DFT computations of the g tensor and that hydrogen bonding influences the g tensor strongly
-
Kaupp M.Remenyi C.Vaara J.Malkina O.L.Malkin V.G.Density functional calculations of electronic g-tensors for semiquinone radical anions. The role of hydrogen bonding and substituent effects J Am Chem Soc 124 2002 2709-2722 This study shows that substituent effects on semiquinones are quantitatively predicted by DFT computations of the g tensor and that hydrogen bonding influences the g tensor strongly.
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(2002)
J Am Chem Soc
, vol.124
, pp. 2709-2722
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Kaupp, M.1
Remenyi, C.2
Vaara, J.3
Malkina, O.L.4
Malkin, V.G.5
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32
-
-
0035857235
-
Influence of solvent polarity and hydrogen bonding on the EPR parameters of a nitroxide spin label studied by 9-GHz and 95-GHz EPR spectroscopy and DFT calculations
-
Hyperfine couplings and g values of nitroxide radicals were measured in solvents of different polarity and different proticity and the two contributions could be unravelled with the help of quantum-chemical computations
-
Owenius R.Engstrom M.Lindgren M.Huber M.Influence of solvent polarity and hydrogen bonding on the EPR parameters of a nitroxide spin label studied by 9-GHz and 95-GHz EPR spectroscopy and DFT calculations J Phys Chem A 105 2001 10967-10977 Hyperfine couplings and g values of nitroxide radicals were measured in solvents of different polarity and different proticity and the two contributions could be unravelled with the help of quantum-chemical computations.
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(2001)
J Phys Chem A
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Owenius, R.1
Engstrom, M.2
Lindgren, M.3
Huber, M.4
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33
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0035894459
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Ab initio calculations of electric field effects on the g-tensor of a nitroxide radical
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Ding Z.Gulla A.F.Budil D.E.Ab initio calculations of electric field effects on the g-tensor of a nitroxide radical J Chem Phys 115 2001 10685-10693
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(2001)
J Chem Phys
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Ding, Z.1
Gulla, A.F.2
Budil, D.E.3
-
34
-
-
0037019650
-
Multifrequency EPR study and density functional g-tensor calculations of persistent organorhenium radical complexes
-
A nice example of how high-field multi-frequency EPR measurements and g tensor computations complement each other
-
Frantz S.Hartmann H.Doslik N.Wanner M.Kaim W.Kummerer H.J.Denninger G.Barra A.L.Duboc-Toia C.Fiedler J.Ciofini I.Urban C.Kaupp M.Multifrequency EPR study and density functional g-tensor calculations of persistent organorhenium radical complexes J Am Chem Soc 124 2002 10563-10571 A nice example of how high-field multi-frequency EPR measurements and g tensor computations complement each other.
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(2002)
J Am Chem Soc
, vol.124
, pp. 10563-10571
-
-
Frantz, S.1
Hartmann, H.2
Doslik, N.3
Wanner, M.4
Kaim, W.5
Kummerer, H.J.6
Denninger, G.7
Barra, A.L.8
Duboc-Toia, C.9
Fiedler, J.10
Ciofini, I.11
Urban, C.12
Kaupp, M.13
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35
-
-
0001686159
-
Calculation of the G-tensor of electron paramagnetic resonance spectroscopy using gauge-including atomic orbitals and density functional theory
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Schreckenbach G.Ziegler T.Calculation of the G-tensor of electron paramagnetic resonance spectroscopy using gauge-including atomic orbitals and density functional theory J Phys Chem A 101 1997 3388-3399
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(1997)
J Phys Chem A
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Schreckenbach, G.1
Ziegler, T.2
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36
-
-
0036605316
-
Calculation of electronic g-tensors for transition metal complexes using hybrid density functionals and atomic meanfield spin-orbit operators
-
Kaupp M.Reviakine R.Malkina O.L.Arbuznikov A.Schimmelpfennig B.Malkin V.G.Calculation of electronic g-tensors for transition metal complexes using hybrid density functionals and atomic meanfield spin-orbit operators J Comput Chem 23 2002 794-803
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J Comput Chem
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Kaupp, M.1
Reviakine, R.2
Malkina, O.L.3
Arbuznikov, A.4
Schimmelpfennig, B.5
Malkin, V.G.6
-
38
-
-
0002180555
-
Electron-paramagnetic-resonance nitroxide spin-labelling of ceramic and metal-oxide surface hydroxyls, and use in studying surface molecular dynamics vs. temperature, solvent, and polymer additive
-
Auteri F.P.Belford R.L.Robinson B.H.Clarkson R.B.Electron-paramagnetic- resonance nitroxide spin-labelling of ceramic and metal-oxide surface hydroxyls, and use in studying surface molecular dynamics vs. temperature, solvent, and polymer additive Coll Surf A 81 1993 25-42
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Coll Surf A
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Auteri, F.P.1
Belford, R.L.2
Robinson, B.H.3
Clarkson, R.B.4
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39
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0029633835
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Polymers at solid interfaces-A spin-labelling approach
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Hommel H.Polymers at solid interfaces-A spin-labelling approach Adv Colloid Interf Sci 54 1995 209-277
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(1995)
Adv Colloid Interf Sci
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Hommel, H.1
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40
-
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0000680098
-
Chain mobility restrictions in random ionomers studied by electron spin resonance spectroscopy
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Tsagaropoulos G.Kim J.S.Eisenberg A.Chain mobility restrictions in random ionomers studied by electron spin resonance spectroscopy Macromolecules 29 1996 2222-2228
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(1996)
Macromolecules
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Tsagaropoulos, G.1
Kim, J.S.2
Eisenberg, A.3
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41
-
-
0031162656
-
EPR studies on telechelic polymers: Characterization of ion multiplets
-
Schädler V.Franck A.Wiesner U.Spiess H.W.EPR studies on telechelic polymers: characterization of ion multiplets Macromolecules 30 1997 3832-3838
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(1997)
Macromolecules
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Schädler, V.1
Franck, A.2
Wiesner, U.3
Spiess, H.W.4
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42
-
-
0029344941
-
Nitroxide spin probe label study of hydrogen-bonding and probe size effects in a linear epoxy polymer
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Pace M.D.Snow A.W.Nitroxide spin probe label study of hydrogen-bonding and probe size effects in a linear epoxy polymer Macromolecules 28 1995 5300-5305
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(1995)
Macromolecules
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Pace, M.D.1
Snow, A.W.2
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43
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0031175489
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Model for the interactions between anionic dendrimers and cationic surfactants by means of the spin probe method
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Ottaviani M.F.Andechaga P.Turro N.J.Tomaglia D.A.Model for the interactions between anionic dendrimers and cationic surfactants by means of the spin probe method J Phys Chem B 101 1997 6057-6065
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J Phys Chem B
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Ottaviani, M.F.1
Andechaga, P.2
Turro, N.J.3
Tomaglia, D.A.4
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44
-
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0343674662
-
13 (Pluronic L64): Hydration, dynamics and order in the polymer aggregates
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13 (Pluronic L64): hydration, dynamics and order in the polymer aggregates Polymer 41 2000 4679-4689
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Polymer
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Zhou, L.1
Schlick, S.2
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45
-
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0036004918
-
Determination of the nanostructure of polymer materials by electron paramagnetic resonance spectroscopy
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Jeschke G.Determination of the nanostructure of polymer materials by electron paramagnetic resonance spectroscopy Macromol Rapid Commun 23 2002 227-246
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(2002)
Macromol Rapid Commun
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Jeschke, G.1
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46
-
-
0037112592
-
Distance measurements in the nanometer range by pulse EPR
-
Jeschke G.Distance measurements in the nanometer range by pulse EPR Chem Phys Chem 3 2002 927-932
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(2002)
Chem Phys Chem
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-
Jeschke, G.1
-
47
-
-
0036290220
-
Direct conversion of EPR dipolar time evolution data to distance distributions
-
Pair correlation functions for EPR spin probes can be computed from experimental data in a model-free approach
-
Jeschke G.Koch A.Jonas U.Godt A.Direct conversion of EPR dipolar time evolution data to distance distributions J Magn Reson 155 2002 72-82 Pair correlation functions for EPR spin probes can be computed from experimental data in a model-free approach.
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(2002)
J Magn Reson
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-
Jeschke, G.1
Koch, A.2
Jonas, U.3
Godt, A.4
-
48
-
-
0037093869
-
Protein structure determination using long-distance constraints from double-quantum coherence ESR: study of T4 lysozyme
-
On the example of a soluble protein with known crystal structure, it is demonstrated that a few long-range distances obtained by EPR measurements constrain the structure of a macromolecule to a large extent
-
Borbat P.P.Mchaourab H.S.Freed J.H.Protein structure determination using long-distance constraints from double-quantum coherence ESR: study of T4 lysozyme J Am Chem Soc 124 2002 5304-5314 On the example of a soluble protein with known crystal structure, it is demonstrated that a few long-range distances obtained by EPR measurements constrain the structure of a macromolecule to a large extent.
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(2002)
J Am Chem Soc
, vol.124
, pp. 5304-5314
-
-
Borbat, P.P.1
Mchaourab, H.S.2
Freed, J.H.3
-
49
-
-
0037131445
-
Selective measurements of a nitroxide-nitroxide separation of 5 nm and a nitroxide-copper separation of 2.5 nm in a terpyridine-based Copper(II) complex by pulse EPR spectroscopy
-
A demonstration that distances between metal centers and nitroxide spin labels can be measured by EPR with high precision
-
Narr E.Godt A.Jeschke G.Selective measurements of a nitroxide-nitroxide separation of 5 nm and a nitroxide-copper separation of 2.5 nm in a terpyridine-based Copper(II) complex by pulse EPR spectroscopy Angew Chem Int Ed 41 2002 3907-3910 A demonstration that distances between metal centers and nitroxide spin labels can be measured by EPR with high precision.
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(2002)
Angew Chem Int Ed
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, pp. 3907-3910
-
-
Narr, E.1
Godt, A.2
Jeschke, G.3
-
50
-
-
0036384679
-
PELDOR at S- and X-band frequencies and the separation of exchange coupling from dipolar coupling
-
Weber A.Schiemann O.Bode B.Prisner T.F.PELDOR at S- and X-band frequencies and the separation of exchange coupling from dipolar coupling J Magn Reson 157 2002 277-285
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(2002)
J Magn Reson
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, pp. 277-285
-
-
Weber, A.1
Schiemann, O.2
Bode, B.3
Prisner, T.F.4
-
51
-
-
0037164101
-
Pulsed electron-electron double resonance on multinuclear metal clusters: Assignment of spin projection factors based on the dipolar interaction
-
Measurements of the dipole-dipole interaction of an observer spin with the effective spin 1/2 of a multinuclear cluster probe the inner structure of this cluster, i.e. the coupling scheme of the spins of which the cluster is composed
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Elsasser C.Brecht M.Bittl R.Pulsed electron-electron double resonance on multinuclear metal clusters: assignment of spin projection factors based on the dipolar interaction J Am Chem Soc 124 2002 12606-12611 Measurements of the dipole-dipole interaction of an observer spin with the effective spin 1/2 of a multinuclear cluster probe the inner structure of this cluster, i.e. the coupling scheme of the spins of which the cluster is composed.
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Elsasser, C.1
Brecht, M.2
Bittl, R.3
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52
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0000242143
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Hyperfine sublevel correlation (HYSCORE) spectroscopy-A 2D electron-spin-resonance investigation of the squaric acid radical
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Hofer P.Grupp A.Nebenfuhr H.Mehring M.Hyperfine sublevel correlation (HYSCORE) spectroscopy-A 2D electron-spin-resonance investigation of the squaric acid radical Chem Phys Lett 132 1986 279-282
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Hofer, P.1
Grupp, A.2
Nebenfuhr, H.3
Mehring, M.4
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53
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0034201416
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Intensity of cross-peaks in HYSCORE spectra of S=1/2, I=1/2 spin systems
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Dikanov S.A.Tyryshkin A.M.Bowman M.K.Intensity of cross-peaks in HYSCORE spectra of S=1/2, I=1/2 spin systems J Magn Reson 144 2000 228-242
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J Magn Reson
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Dikanov, S.A.1
Tyryshkin, A.M.2
Bowman, M.K.3
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54
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0035367368
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Multiple quantum coherence in HYSCORE spectra
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By the use of pulse matching, multiple-quantum cross-peaks can be significantly enhanced in HYSCORE spectra and additional information as well as better resolution are gained
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Liesum L.Schweiger A.Multiple quantum coherence in HYSCORE spectra J Chem Phys 114 2001 9478-9488 By the use of pulse matching, multiple-quantum cross-peaks can be significantly enhanced in HYSCORE spectra and additional information as well as better resolution are gained.
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(2001)
J Chem Phys
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, pp. 9478-9488
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Liesum, L.1
Schweiger, A.2
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55
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0003454218
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Two-dimensional pulsed TRIPLE at 95 GHz
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This experiment may be used to unravel ENDOR spectra due to different sites in a single crystal and possibly to obtain information on the relative orientation of electron-nuclear spin vectors in the same paramagnetic center
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Epel B.Goldfarb D.Two-dimensional pulsed TRIPLE at 95 GHz J Magn Reson 146 2000 196-203 This experiment may be used to unravel ENDOR spectra due to different sites in a single crystal and possibly to obtain information on the relative orientation of electron-nuclear spin vectors in the same paramagnetic center.
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(2000)
J Magn Reson
, vol.146
, pp. 196-203
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Epel, B.1
Goldfarb, D.2
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56
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0035935964
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Right-angle wiggling electron paramagnetic resonance spectroscopy
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Separation of anisotropic from isotropic contributions to the resonance frequencies by a method that is technically not too demanding and provides substantial resolution enhancements for solid-state measurements on transition metal complexes
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Eichel R.A.Schweiger A.Right-angle wiggling electron paramagnetic resonance spectroscopy J Chem Phys 115 2001 9126-9135 Separation of anisotropic from isotropic contributions to the resonance frequencies by a method that is technically not too demanding and provides substantial resolution enhancements for solid-state measurements on transition metal complexes.
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(2001)
J Chem Phys
, vol.115
, pp. 9126-9135
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Eichel, R.A.1
Schweiger, A.2
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