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1
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0028281579
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D. E. Robertson, R. S. Farid, C. C. Moser, J. L. Urbauer, S. E. Mulholland, R. Pidikiti, J. D. Lear, A. J. Wand, W. F. DeGrado, and P. L. Dutton, Nature, 368, 425 (1994).
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(1994)
Nature
, vol.368
, pp. 425
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Robertson, D.E.1
Farid, R.S.2
Moser, C.C.3
Urbauer, J.L.4
Mulholland, S.E.5
Pidikiti, R.6
Lear, J.D.7
Wand, A.J.8
DeGrado, W.F.9
Dutton, P.L.10
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2
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37049076968
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H. Mihara, Y. Tanaka, T. Fujimoto, and N. Nishino, J. Chem. Soc., Perkin Trans. 2, 1995, 1133;
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J. Chem. Soc., Perkin Trans. 2
, vol.1995
, pp. 1133
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Mihara, H.1
Tanaka, Y.2
Fujimoto, T.3
Nishino, N.4
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3
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37049076968
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in press and references cited therein
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H. Mihara, Y. Tanaka, T. Fujimoto, and N. Nishino, J. Chem. Soc., Perkin Trans. 2, 1995, in press and references cited therein.
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J. Chem. Soc., Perkin Trans. 2
, vol.1995
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Mihara, H.1
Tanaka, Y.2
Fujimoto, T.3
Nishino, N.4
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4
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20544457478
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The porphyrin was synthesized by the reported procedure by N. Nishino, Kyushu Institute of Technology
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The porphyrin was synthesized by the reported procedure by N. Nishino, Kyushu Institute of Technology.
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5
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20544470380
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note
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Acm, acetamidomethyl; Boc, t-butyloxycarbonyl; ClZ, 2-chlorobenzyloxycarbonyl; Fmoc, 9-fluorenylmethyloxycarbonyl; Trt, trityl. The synthetic details will be reported elsewhere.
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6
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37049081050
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N. Fujii, A. Otaka, O. Ikemura, K. Akaji, S. Funakoshi, Y. Hayashi, Y. Kuroda, and H. Yajima, J. Chem. Soc., Chem. Commun., 1987, 274.
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J. Chem. Soc., Chem. Commun.
, vol.1987
, pp. 274
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Fujii, N.1
Otaka, A.2
Ikemura, O.3
Akaji, K.4
Funakoshi, S.5
Hayashi, Y.6
Kuroda, Y.7
Yajima, H.8
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7
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0001255839
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S. Matile, N. Berova, K. Nakanishi, S. Novkova, I. Philipova, and B. Blagoev, J. Am. Chem. Soc., 117, 7021 (1995).
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(1995)
J. Am. Chem. Soc.
, vol.117
, pp. 7021
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Matile, S.1
Berova, N.2
Nakanishi, K.3
Novkova, S.4
Philipova, I.5
Blagoev, B.6
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8
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20544437583
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note
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7 λmax (e)/buffer 407 nm (43500), 424 (47500), 518 (4000), 555 (1500), 593 (1500), and 645 (1500) for Por1α; 406 (75000), 423 (87000), 517 (5000), 556 (2000), 595 (2000), and 651 (2000) for Por2α. λmax (ε)/TFE 413 nm (279000), 516 (9500), 552 (6000), 589 (4500), and 636 (4000) for Por1α; 413 (547000), 517 (18000), 553 (15000), 589 (14000), 639 (15000) for Por2α; 413 nm (353000), 516 (15200), 553 (10800), 585 (10000), and 637 (10200) for the porphyrin. Fluorescence emissions were at 654 nm (relative intensity 1.0) in buffer and 645 nm (relative intensity 16.0) in TFE for all porphyrins.
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