12 Inter-spin Interactions of Organic Radical Chains in Organic 1D. . .
461
38. H. Kobayashi, T. Ueda, K. Miyakubo, J. Toyoda, T. Eguchi, A. Tani, Preparation and
characterization of new inclusion compound with 1D molecular arrangement of organic
radicals using a one-dimensional organic homogeneous nanochannel template. J Mater Chem
15, 872 (2005)
39. H. Kobayashi, T. Ueda, K. Miyakubo, T. Eguchi, A. Tani, Spin-spin interaction of TEMPO
molecular chains formed in an organic one-dimensional nanochannel as studied by electron
spin resonance (ESR). Bull Chem Soc Jpn 80, 711 (2007)
40. H. Kobayashi, T. Ueda, K. Miyakubo, T. Eguchi, A. Tani, ESR study of molecular dynamics
and orientation of TEMPO included in organic one-dimensional nanochannel. Phys Chem
Chem Phys 10, 1263 (2008)
41. H. Kobayashi, K. Takeuchi, T. Asaji, Molecular orientation and dynamics of different sized
radicals included in organic 1-D nanochannels. J Phys Chem A 117, 2093 (2013)
42. H. Kobayashi, T. Asaji, A. Tani, Preparation and characterization of new inclusion compounds
using stable nitroxide radicals and an organic 1-D nanochannel as a template. Materials 3, 3625
(2010)
43. H. Kobayashi, K. Aoki, T. Asaji, Dynamics of TEMPOL radicals in TPP 1D nanochannels and
different molecular orientation from other TEMPO derivatives. Chem Lett 44, 893 (2015)
44. H. Kobayashi, T. Mori, Y. Morinaga, E. Fujimori, K. Akiniwa, F. Iwahori, Electron spin
resonance study of molecular orientation and dynamics of phenyl imino and nitronyl nitroxide
radicals in organic 1D nanochannels of Tris(o-phenylenedioxy)cyclotriphosphazene. J Phys
Chem A 122, 5493 (2018)
45. J.H Freed, Spin labeling, theory and applications, ed. by L. J Berliner (Academic, New York,
1976)
46. S. Stoll, A. Schweiger, EasySpin, a comprehensive software package for spectral simulation
and analysis in EPR. J Magn Reson 178, 42 (2006)
47. http://www.easyspin.org/: see the manual of Chili (2018–12–07)
48. B. Dzikovski, D. Tipikin, V. Livshits, K. Earle, J. Freed, Multifrequency ESR study of spinlabeled molecules in inclusion compounds with cyclodextrins. Phys Chem Chem Phys 11, 6676
(2009)
49. C. Aliaga, F. Bravo-Moraga, D. Gonzalez-Nilo, S. Márquez, S. Lühr, G. Mena, M.C. Rezende,
Location of TEMPO derivatives in micelles: subtle effect of the probe orientation. Food Chem
192, 395 (2016)
50. R.K.R. Jetti, P.K. Thallapally, F. Xue, T.C.W. Mak, A. Nangia, Hexagonal nanoporous
host structures based on 2,4,6-tris-4-(halo-phenoxy)-1,3,5-triazines (halo = chloro, bromo).
Tetrahedron 56, 6707 (2000)
51. H. Kobayashi, T. Asaji, A. Tani, ESR study of the molecular orientation and dynamics of stable
organic radicals included in the 1-D organic nanochannels of 2,4,6-tris-4-(chlorophenoxy)1,3,5-triazine. Magn Reson Chem 50, 221 (2012)
52. H. Kobayashi, Y. Furuhashi, H. Nakagawa, T. Asaji, ESR study of molecular orientation and
dynamics of TEMPO derivatives in CLPOT 1D nanochannels. Magn Reson Chem 54, 641
(2016)
53. H. Kobayashi, H. Takamisawa, Y. Furuhashi, H. Nakagawa, K. Nakatsugawa, K. Takeuchi, Y.
Morinaga, Inter-spin interaction of CLPOT inclusion compounds with 1D molecular chains
of 4-X-TEMPO radicals in the temperature range of 4.2-300 K. Bull Chem Soc Jpn 91, 375
(2018)
54. M. Bonin, G. Labat, G. Couderc, T.A. Lüthi, K. Reichenbächer, J. Hulliger, H.–.B. Bürgi,
Novel host-guest structures of 2,4,6-Tris(4-Halophenoxy)-1,3,5-Triazines (XPOT): inclusion
of C 60 and pyridine. J Chem Crystllogr 42, 645 (2012)
55. H.I. Süss, J. Hulliger, Organic channel inclusion compound featuring an open pore size of 12
Å. Microporous Mesoporous Mater 78, 23 (2005)
56. B. Naydenov, C. Spudat, W. Harneit, H.I. Süss, J. Hulliger, J. Nuss, M. Jansen, Ordered
inclusion of endohedral fullerenes N@C 60 and P@C 60 in a crystalline matrix. Chem. Phys.
Lett 424, 327 (2006). S.D. Bruce, J. Higinbotham, I. Marshall, P.H. Beswick, An Analytical
Derivation of a Popular Approximation of the Voigt Function for Quantification of NMR
Spectra. J Magn Reson 142, 57 (2000)
461
38. H. Kobayashi, T. Ueda, K. Miyakubo, J. Toyoda, T. Eguchi, A. Tani, Preparation and
characterization of new inclusion compound with 1D molecular arrangement of organic
radicals using a one-dimensional organic homogeneous nanochannel template. J Mater Chem
15, 872 (2005)
39. H. Kobayashi, T. Ueda, K. Miyakubo, T. Eguchi, A. Tani, Spin-spin interaction of TEMPO
molecular chains formed in an organic one-dimensional nanochannel as studied by electron
spin resonance (ESR). Bull Chem Soc Jpn 80, 711 (2007)
40. H. Kobayashi, T. Ueda, K. Miyakubo, T. Eguchi, A. Tani, ESR study of molecular dynamics
and orientation of TEMPO included in organic one-dimensional nanochannel. Phys Chem
Chem Phys 10, 1263 (2008)
41. H. Kobayashi, K. Takeuchi, T. Asaji, Molecular orientation and dynamics of different sized
radicals included in organic 1-D nanochannels. J Phys Chem A 117, 2093 (2013)
42. H. Kobayashi, T. Asaji, A. Tani, Preparation and characterization of new inclusion compounds
using stable nitroxide radicals and an organic 1-D nanochannel as a template. Materials 3, 3625
(2010)
43. H. Kobayashi, K. Aoki, T. Asaji, Dynamics of TEMPOL radicals in TPP 1D nanochannels and
different molecular orientation from other TEMPO derivatives. Chem Lett 44, 893 (2015)
44. H. Kobayashi, T. Mori, Y. Morinaga, E. Fujimori, K. Akiniwa, F. Iwahori, Electron spin
resonance study of molecular orientation and dynamics of phenyl imino and nitronyl nitroxide
radicals in organic 1D nanochannels of Tris(o-phenylenedioxy)cyclotriphosphazene. J Phys
Chem A 122, 5493 (2018)
45. J.H Freed, Spin labeling, theory and applications, ed. by L. J Berliner (Academic, New York,
1976)
46. S. Stoll, A. Schweiger, EasySpin, a comprehensive software package for spectral simulation
and analysis in EPR. J Magn Reson 178, 42 (2006)
47. http://www.easyspin.org/: see the manual of Chili (2018–12–07)
48. B. Dzikovski, D. Tipikin, V. Livshits, K. Earle, J. Freed, Multifrequency ESR study of spinlabeled molecules in inclusion compounds with cyclodextrins. Phys Chem Chem Phys 11, 6676
(2009)
49. C. Aliaga, F. Bravo-Moraga, D. Gonzalez-Nilo, S. Márquez, S. Lühr, G. Mena, M.C. Rezende,
Location of TEMPO derivatives in micelles: subtle effect of the probe orientation. Food Chem
192, 395 (2016)
50. R.K.R. Jetti, P.K. Thallapally, F. Xue, T.C.W. Mak, A. Nangia, Hexagonal nanoporous
host structures based on 2,4,6-tris-4-(halo-phenoxy)-1,3,5-triazines (halo = chloro, bromo).
Tetrahedron 56, 6707 (2000)
51. H. Kobayashi, T. Asaji, A. Tani, ESR study of the molecular orientation and dynamics of stable
organic radicals included in the 1-D organic nanochannels of 2,4,6-tris-4-(chlorophenoxy)1,3,5-triazine. Magn Reson Chem 50, 221 (2012)
52. H. Kobayashi, Y. Furuhashi, H. Nakagawa, T. Asaji, ESR study of molecular orientation and
dynamics of TEMPO derivatives in CLPOT 1D nanochannels. Magn Reson Chem 54, 641
(2016)
53. H. Kobayashi, H. Takamisawa, Y. Furuhashi, H. Nakagawa, K. Nakatsugawa, K. Takeuchi, Y.
Morinaga, Inter-spin interaction of CLPOT inclusion compounds with 1D molecular chains
of 4-X-TEMPO radicals in the temperature range of 4.2-300 K. Bull Chem Soc Jpn 91, 375
(2018)
54. M. Bonin, G. Labat, G. Couderc, T.A. Lüthi, K. Reichenbächer, J. Hulliger, H.–.B. Bürgi,
Novel host-guest structures of 2,4,6-Tris(4-Halophenoxy)-1,3,5-Triazines (XPOT): inclusion
of C 60 and pyridine. J Chem Crystllogr 42, 645 (2012)
55. H.I. Süss, J. Hulliger, Organic channel inclusion compound featuring an open pore size of 12
Å. Microporous Mesoporous Mater 78, 23 (2005)
56. B. Naydenov, C. Spudat, W. Harneit, H.I. Süss, J. Hulliger, J. Nuss, M. Jansen, Ordered
inclusion of endohedral fullerenes N@C 60 and P@C 60 in a crystalline matrix. Chem. Phys.
Lett 424, 327 (2006). S.D. Bruce, J. Higinbotham, I. Marshall, P.H. Beswick, An Analytical
Derivation of a Popular Approximation of the Voigt Function for Quantification of NMR
Spectra. J Magn Reson 142, 57 (2000)