Home / Publications / Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin

Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin

Nikolay Mikhailovich Loim 1
Nikolay Mikhailovich Loim
, 
Natalya Vladimirovna Abramova 1
Natalya Vladimirovna Abramova
, 
Vyacheslav Ivanovich Sokolov 1
Vyacheslav Ivanovich Sokolov
10.1070/MC1996v006n02ABEH000572
Published 1996-04-30
Communication , Volume 6, Issue 2, 46-47
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Loim N. M., Abramova N. V., Sokolov V. I. Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin // Mendeleev Communications. 1996. Vol. 6. No. 2. pp. 46-47.
GOST all authors (up to 50) Copy
Loim N. M., Abramova N. V., Sokolov V. I. Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin // Mendeleev Communications. 1996. Vol. 6. No. 2. pp. 46-47.
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TY - JOUR
DO - 10.1070/MC1996v006n02ABEH000572
UR - https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000572
TI - Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin
T2 - Mendeleev Communications
AU - Loim, Nikolay Mikhailovich
AU - Abramova, Natalya Vladimirovna
AU - Sokolov, Vyacheslav Ivanovich
PY - 1996
DA - 1996/04/30
PB - Mendeleev Communications
SP - 46-47
IS - 2
VL - 6
ER -
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@article{1996_Loim,
author = {Nikolay Mikhailovich Loim and Natalya Vladimirovna Abramova and Vyacheslav Ivanovich Sokolov},
title = {Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin},
journal = {Mendeleev Communications},
year = {1996},
volume = {6},
publisher = {Mendeleev Communications},
month = {Apr},
url = {https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000572},
number = {2},
pages = {46--47},
doi = {10.1070/MC1996v006n02ABEH000572}
}
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Loim, Nikolay Mikhailovich, et al. “Synthesis of 5,10,15,20-tetra(ruthenocenyl)porphyrin and 5,10,15,20-tetra(ferrocenyl)porphyrin.” Mendeleev Communications, vol. 6, no. 2, Apr. 1996, pp. 46-47. https://mendcomm.colab.ws/publications/10.1070/MC1996v006n02ABEH000572.

Abstract

Using the Lindsey method the title compounds were prepared from the corresponding metallocenecarbaldehydes and pyrrole in 56% and 40% yield respectively.

References

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10.1070/MC1996v006n02ABEH000572_bib3
Loim
Izv. Akad. Nauk, Ser. Khim., 1994
4.
10.1070/MC1996v006n02ABEH000572_bib4
Loim
Izv. Akad. Nauk, Ser. Khim., 1994
6.
Inter- and intramolecular quenching of the singlet excited state of porphyrins by ferrocene
Giasson R., Lee E.J., Zhao X., Wrighton M.S.
The Journal of Physical Chemistry, 1993
8.
Investigation of the synthesis of ortho-substituted tetraphenylporphyrins
Lindsey J.S., Wagner R.W.
Journal of Organic Chemistry, 1989