Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model, redox-active complexes for molecular electronics
Avoiding problem reactions at the ferrocenyl-alkyne motif: a convenient synthesis of model,
redox-active complexes for molecular electronics - Dalton Transactions (RSC Publishing) …
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 …
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 …
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 …
accessible</italic> thiolates on the aryl ring is reported. Unanticipated reactions between …