Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model, redox-active complexes for molecular electronics

MS Inkpen, AJP White, T Albrecht, NJ Long - Dalton Transactions, 2014 - pubs.rsc.org
Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model,
redox-active complexes for molecular electronics - Dalton Transactions (RSC Publishing) …

Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model, redox-active complexes for molecular electronics.

MS Inkpen, AJ White, T Albrecht… - Dalton Transactions …, 2014 - europepmc.org
Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model,
redox-active complexes for molecular electronics. - Abstract - Europe PMC Sign in | Create an …

Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model, redox-active complexes for molecular electronics

MS Inkpen, AJP White, T Albrecht… - Dalton transactions …, 2014 - pubmed.ncbi.nlm.nih.gov
Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model,
redox-active complexes for molecular electronics Avoiding problem reactions at the …

Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model, redox-active complexes for molecular electronics

MS Inkpen, AJP White, T Albrecht, NJ Long - Dalton Trans., 2014 - cir.nii.ac.jp
抄録< p> A much improved route to 1, 1′-bis (arylethynyl) ferrocenes comprising< italic>
accessible</italic> thiolates on the aryl ring is reported. Unanticipated reactions between …