Differential quenching of the angular momentum of the B and Q bands of a porphyrin as a result of extended ring π-conjugation

Abstract

A novel porphyrin, whose [Formula: see text]-system has been extended via the presence of two additional carbon–carbon triple bonds on opposite meso-positions and by fusion of a single naphthalene unit simultaneously bridging the third meso-position and the [Formula: see text]-carbon of one of the pyrroles, has been synthesized in good yield. Absorption, magnetic circular dichroism, emission, and theoretical spectra are reported for the fused and unfused trans-naphthalene free base and zinc porphyrins. The fusing of one of the naphthalene moieties results in significant changes to the absorption spectrum and, very unusually, the bridged meso-[Formula: see text]-pyrrole fusion results in quenching of the MCD Faraday pseudo-A term in the porphyrin’s B band (S2). This unique effect was interpreted as resulting from the origin of the electronic structure of the second excited state (the B state). The [Formula: see text] and [Formula: see text] polarizations are completely mixed by the electronic effects of the non-symmetric extended conjugation of the [Formula: see text] ring. Analysis of the origin of the MCD signal indicates that the presence of this novel mixed polarization leads to negligible angular momentum in the important B state. To our knowledge, this is the first report in which the magnetic moment in a porphyrin’s intensely absorbing B band has been quenched while the angular momentum in the Q band, the first excited state, remains as normal. This implies that the photophysical properties of the B state are likely very different than those of the Q state, which has novel and significant implications for applications, especially in non-linear spectroscopy.