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Synthetic Methodology for Asymmetric Ferrocene Derived Bio-conjugate Systems via Solid Phase Resin-based Methodology
Published on: March 12, 2015
Macrocyclic core size limit for stabilizing ferrocenoporphyrinoids
Suman Das1, Gunasekaran Velmurugan2, Harapriya Rath1
1School of Chemical Sciences, Indian Association for the Cultivation of Science, 2A/2B Raja SC Mullick Road, Jadavpur, Kolkata 700 032, India. ichr@iacs.res.in.
None:
Incorporation of 1,1'-substitued ferrocene into the macrocyclic π-conjugation pathways of corrole and subporphyrin leads to unprecedented rupture of the ferrocene unit with structural isolation of a dicyclopentadiene bridged porphyrinoid and a 1,3,4 trichloro-6a,6b,9,9a,10,10a-hexahydro-6H-6,10 methanopentaleno[1,2-c] chromen-2-ol-bridged porphyrinoid, respectively, both of which lack global macrocyclic π-conjugation.
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