Abstract
The low and high-resolution mass spectra and the spectra of the metastable ions (DADI) of a number of porphyrins and their copper complexes with −CR=N−R, −CH2NHR, and −CH2NRR substituents in the meso position of the porphyrin ring were investigated. The principal pathways of fragmentation of the meso-substituted porphyrins were established.
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See [1] for communication VI.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 773–779, June, 1978.
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Ponomarev, G.V., Suboch, V.P. & Lyashko, A.N. Porphyrins. Chem Heterocycl Compd 14, 631–636 (1978). https://doi.org/10.1007/BF00481136
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DOI: https://doi.org/10.1007/BF00481136