Naphthalene Exchange in [Re(η6‐napht)2]+ with Pharmaceuticals Leads to Highly Functionalized Sandwich Complexes [M(η6‐pharm)2]+ (M=Re/99mTc). Issue 5 (13th December 2021)
- Record Type:
- Journal Article
- Title:
- Naphthalene Exchange in [Re(η6‐napht)2]+ with Pharmaceuticals Leads to Highly Functionalized Sandwich Complexes [M(η6‐pharm)2]+ (M=Re/99mTc). Issue 5 (13th December 2021)
- Main Title:
- Naphthalene Exchange in [Re(η6‐napht)2]+ with Pharmaceuticals Leads to Highly Functionalized Sandwich Complexes [M(η6‐pharm)2]+ (M=Re/99mTc)
- Authors:
- Nadeem, Qaisar
Battistin, Federica
Blacque, Olivier
Alberto, Roger - Abstract:
- Abstract: Bis‐arene sandwich complexes are generally prepared by the Fischer‐Hafner reaction, which conditions are incompatible with most O‐ and N‐ functional groups. We report a new way for the synthesis of sandwich type complexes [Re(η 6 ‐arene)2 ] + and [Re(η 6 ‐arene)(η 6 ‐benzene)] + from [Re(η 6 ‐napht)2 ] + and [Re(η 6 ‐napht)(η 6 ‐benzene)] +, with functionalized arenes and pharmaceuticals. N‐methylpyrrolidine (NMP) facilitates the substitution of naphthalene with the incoming arene. A series of fully characterized rhenium sandwich complexes with simple arenes, such as aniline, as well as with active compounds like lidocaine and melatonin are presented. With these rhenium compounds in hand, the radioactive sandwich complexes [ 99m Tc(η 6 ‐pharm)2 ] + (pharm=pharmaceutical) can be unambiguously confirmed. The direct labelling of pharmaceuticals with 99m Tc through η 6 ‐coordination to phenyl rings and the confirmation of the structures with the rhenium homologues opens a path into molecular theranostics. Abstract : To overcome the limits of the Fischer‐Hafner reaction, [Re(η 6 ‐napht)2 ] + and [Re(η 6 ‐napht)(benzene)] + have been used to prepare sandwich complexes [Re(η 6 ‐arene)2 ] + and [Re(η 6 ‐arene)(η 6 ‐benzene)] + . NMP is used to promote the substitution of naphthalene with simple arenes as well as with active compounds like lidocaine and melatonin. This compound can be used to unambiguously confirm the radioactive sandwich complexes [ 99m Tc(η 6 ‐pharm)2 ] +Abstract: Bis‐arene sandwich complexes are generally prepared by the Fischer‐Hafner reaction, which conditions are incompatible with most O‐ and N‐ functional groups. We report a new way for the synthesis of sandwich type complexes [Re(η 6 ‐arene)2 ] + and [Re(η 6 ‐arene)(η 6 ‐benzene)] + from [Re(η 6 ‐napht)2 ] + and [Re(η 6 ‐napht)(η 6 ‐benzene)] +, with functionalized arenes and pharmaceuticals. N‐methylpyrrolidine (NMP) facilitates the substitution of naphthalene with the incoming arene. A series of fully characterized rhenium sandwich complexes with simple arenes, such as aniline, as well as with active compounds like lidocaine and melatonin are presented. With these rhenium compounds in hand, the radioactive sandwich complexes [ 99m Tc(η 6 ‐pharm)2 ] + (pharm=pharmaceutical) can be unambiguously confirmed. The direct labelling of pharmaceuticals with 99m Tc through η 6 ‐coordination to phenyl rings and the confirmation of the structures with the rhenium homologues opens a path into molecular theranostics. Abstract : To overcome the limits of the Fischer‐Hafner reaction, [Re(η 6 ‐napht)2 ] + and [Re(η 6 ‐napht)(benzene)] + have been used to prepare sandwich complexes [Re(η 6 ‐arene)2 ] + and [Re(η 6 ‐arene)(η 6 ‐benzene)] + . NMP is used to promote the substitution of naphthalene with simple arenes as well as with active compounds like lidocaine and melatonin. This compound can be used to unambiguously confirm the radioactive sandwich complexes [ 99m Tc(η 6 ‐pharm)2 ] + . … (more)
- Is Part Of:
- Chemistry. Volume 28:Issue 5(2022)
- Journal:
- Chemistry
- Issue:
- Volume 28:Issue 5(2022)
- Issue Display:
- Volume 28, Issue 5 (2022)
- Year:
- 2022
- Volume:
- 28
- Issue:
- 5
- Issue Sort Value:
- 2022-0028-0005-0000
- Page Start:
- n/a
- Page End:
- n/a
- Publication Date:
- 2021-12-13
- Subjects:
- bioorganometallics -- rhenium -- sandwich complexes -- technetium -- theranostics
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.202103566 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 26296.xml