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Christian Slugovc

Publications and source records attributed to Christian Slugovc.

2 recordsLinked to original sources

Molecular fluorescent pH-probes based on 8-hydroxyquinoline.

Three 5,7-pi-extended 8-benzyloxyquinolines, namely 5,7-diphenyl-, 5,7-bis(biphenyl-4-yl)- and 5,7-bis(4-dibenzothiophenyl)-8-benzyloxyquinoline were prepared and investigated as fluorescent pH-probes in nonaqueous solution. Absorption and photoluminescence spectra of the introduced compounds also including the starting material 8-benzyloxy-5,7-dibromoquinoline as well as their N-protonated counterparts were recorded and the results were rationalized by quantum-chemical calculations. A pronounced red shift of the emission occurred upon protonation of the non halogenated derivatives, while the dibromo-derivative is hardly emissive and is virtually not protonated under the conditions used. The diphenyl- and the bis(biphenyl)-derivative especially show promising photoluminescence quantum yields both in the parent and the protonated state making them candidates for the active component in pH sensing applications.

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Labile Complexes of the [RuTp(pn)](+) (Tp = Tripyrazolylborate, pn = Ph(2)PCH(2)CH(2)NMe(2)) Fragment Including the Dinitrogen Ligand(1).

The [TpRu(pn)](+) fragment (Tp = tripyrazolyl, pn = Ph(2)PCH(2)CH(2)NMe(2)), featuring a strong sigma acceptor and a weak pi donor, forms reversible complexes with a variety of sigma donor ligands L including N(2) which appears to be more strongly bonded than even CH(3)CN. X-ray crystal structures of the complexes with L = H(2)O, acetone, CO, N(2), and vinylidene are included (adding to that for L = CH(3)CN from former work), as well as a comparative MO study on the bonding nature of L. The sequence of complex stabilities of [TpRu(pn)L](+) is CF(3)SO(3)(-) < acetone approximately H(2)O < CH(3)CN < N(2) < CO < vinylidene as suggested from EHMO calculations and crystallographic data as well as qualitative experimental results. Despite the notable stability of [TpRu(pn)(eta(1)-N(2))](+), the N-N bond length is 1.097(5) Å, exactly that in free N(2). Our analysis suggests that the insensitivity of the N-N bond essentially originates from the counterbalance of pi bond weakening (through back-donation) and sigma bond strengthening (through reducing the antibonding character of the sigma (2sigma(u)) MO in molecular dinitrogen.

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