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39
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13944264052
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note
-
GPC measurement of 7 was carried out by changing the concentration in the range 0.1 mM to 3.1 μM ([2(Zn)]). No appreciable difference in the peak position and the shape was observed, indicating that the intermolecular interaction can be negligible in the concentration range examined.
-
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40
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13944249638
-
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note
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3protons of 5(Zn) are also shifted to higher field caused by slipped cofacial dimer formation and appeared at 5.48 and 1.72 ppm, respectively (Figure 5b).
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Methanol weakly competes with the imidazolyl group for the coordination to the zinc(II) and thus accelerates the exchanging of the partner in the complementary coordination.
-
-
-
-
50
-
-
13944276841
-
-
note
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3 protons at 3.3 ppm and the presence of β-pyrrole protons at around 5.4 ppm strongly suggest that all of the imidazolylporphyrinatozinc(II) in trisporphyrin formed a complementary dimer and the absence of noncyclic structure in the mixture of larger rings.
-
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51
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-
13944251460
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note
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(10-mer) instead of the average size of rings by using the molecular model (Figure S9).
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