Copper-assisted azide–alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates. Issue 2 (8th November 2016)
- Record Type:
- Journal Article
- Title:
- Copper-assisted azide–alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates. Issue 2 (8th November 2016)
- Main Title:
- Copper-assisted azide–alkyne cycloaddition chemistry as a tool for the production of emissive boron difluoride 3-cyanoformazanates
- Authors:
- Barbon, Stephanie M.
Novoa, Samantha
Bender, Desiree
Groom, Hilary
Luyt, Leonard G.
Gilroy, Joe B. - Abstract:
- Abstract : Emissive BF2 complexes of 3-cyanoformazanates produced using CuAAC chemistry are described. Highlights include ferrocene-substituted derivatives with 'turn-on' fluorescence upon oxidation and a water soluble derivative with application as a cell-imaging agent. Abstract : The synthesis and characterization of emissive boron difluoride (BF2 ) complexes of 3-cyanoformazanate ligands produced using copper-assisted azide–alkyne cycloaddition (CuAAC) chemistry is described. Detailed spectroscopic and electrochemical characterization of benzyl-functionalized complexes served as models and demonstrated that triazole formation at the N -aryl substituents of the formazanate ligand scaffold led to red-shifted absorption and emission maxima and more difficult electrochemical reduction compared to alkyne-substituted precursors. CuAAC chemistry was also used to append ferrocene and tetraethylene glycol substituents to the formazanate backbone. In the case of the ferrocene-substituted complexes, fluorescence was quenched and a reversible oxidation feature (in addition to the reduction features associated with formazanate complexes) was observed using cyclic voltammetry. Treatment with NOBF4 oxidized ferrocene to ferrocenium and resulted in the reestablishment of fluorescence. Tetraethylene glycol substitution produced the first water soluble BF2 formazanate, which was shown to distribute throughout the cytoplasm and nucleus of mouse fibroblast cells when studied as aAbstract : Emissive BF2 complexes of 3-cyanoformazanates produced using CuAAC chemistry are described. Highlights include ferrocene-substituted derivatives with 'turn-on' fluorescence upon oxidation and a water soluble derivative with application as a cell-imaging agent. Abstract : The synthesis and characterization of emissive boron difluoride (BF2 ) complexes of 3-cyanoformazanate ligands produced using copper-assisted azide–alkyne cycloaddition (CuAAC) chemistry is described. Detailed spectroscopic and electrochemical characterization of benzyl-functionalized complexes served as models and demonstrated that triazole formation at the N -aryl substituents of the formazanate ligand scaffold led to red-shifted absorption and emission maxima and more difficult electrochemical reduction compared to alkyne-substituted precursors. CuAAC chemistry was also used to append ferrocene and tetraethylene glycol substituents to the formazanate backbone. In the case of the ferrocene-substituted complexes, fluorescence was quenched and a reversible oxidation feature (in addition to the reduction features associated with formazanate complexes) was observed using cyclic voltammetry. Treatment with NOBF4 oxidized ferrocene to ferrocenium and resulted in the reestablishment of fluorescence. Tetraethylene glycol substitution produced the first water soluble BF2 formazanate, which was shown to distribute throughout the cytoplasm and nucleus of mouse fibroblast cells when studied as a fluorescence imaging agent. … (more)
- Is Part Of:
- Organic chemistry frontiers. Volume 4:Issue 2(2017)
- Journal:
- Organic chemistry frontiers
- Issue:
- Volume 4:Issue 2(2017)
- Issue Display:
- Volume 4, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 2
- Issue Sort Value:
- 2017-0004-0002-0000
- Page Start:
- 178
- Page End:
- 190
- Publication Date:
- 2016-11-08
- Subjects:
- Chemistry, Organic -- Periodicals
547.005 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/qo#!recentarticles&all ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6qo00640j ↗
- Languages:
- English
- ISSNs:
- 2052-4110
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6287.121000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 298.xml