Boron complexes of aromatic ring fused iminopyrrolyl ligands: synthesis, structure, and luminescence properties. Issue 39 (15th September 2016)
- Record Type:
- Journal Article
- Title:
- Boron complexes of aromatic ring fused iminopyrrolyl ligands: synthesis, structure, and luminescence properties. Issue 39 (15th September 2016)
- Main Title:
- Boron complexes of aromatic ring fused iminopyrrolyl ligands: synthesis, structure, and luminescence properties
- Authors:
- Suresh, D.
Ferreira, Bruno
Lopes, Patrícia S.
Gomes, Clara S. B.
Krishnamoorthy, Paramasivam
Charas, Ana
Vila-Viçosa, Diogo
Morgado, Jorge
Calhorda, Maria José
Maçanita, António L.
Gomes, Pedro T. - Abstract:
- Abstract : New fluorescent aromatic ring-fused 2-iminopyrrolyl diphenyl boron complexes are emitters in the range blue to orange. Abstract : The condensation reactions of 2-formylindole (1 ) or 2-formylphenanthro[9, 10- c ]pyrrole (2 ) with various aromatic amines afforded the corresponding phenyl or phenanthrene ring fused mono-/bis-iminopyrrole ligand precursors3–8, which, upon reaction with BPh3 in an appropriate molar ratio, led to the new mono- and diboron chelate compounds Ph2 B[NC8 H5 C(H) N -2, 6-Ar] (Ar = 2, 6-iPr2 C6 H3 9 ; C6 H5 10 ), Ph2 B[(NC8 H5 C(H)N)2 -1, 4-C6 H4 ]BPh2 11, Ph2 B(NC16 H9 C(H) N -Ar) (Ar = 2, 6-iPr2 C6 H3 12 ; C6 H5 13 ), and Ph2 B[(NC16 H9 C(H)N)2 -1, 4-C6 H4 ]BPh2 14, respectively. Boron complexes12–14, containing a phenanthrene fragment fused to the pyrrolyl C3–C4 bond, are highly fluorescent in solution, with quantum efficiencies of 37%, 61% and 58% (in THF), respectively, their emission colours ranging from blue to orange depending on the extension of π-conjugation. Complexes9–11, containing a benzene fragment fused to the pyrrolyl C4–C5 bond, are much weaker emitters, exhibiting quantum efficiencies of 10%, 7% and 6%, respectively. DFT and TDDFT calculations showed that 2, 6-iPr2 C6 H3 N -substituents or, to a smaller extent, the indolyl group prevent a planar geometry of the ligand in the excited state and reveal the existence of a low energy weak band in all the indolyl complexes, which is responsible for the different opticalAbstract : New fluorescent aromatic ring-fused 2-iminopyrrolyl diphenyl boron complexes are emitters in the range blue to orange. Abstract : The condensation reactions of 2-formylindole (1 ) or 2-formylphenanthro[9, 10- c ]pyrrole (2 ) with various aromatic amines afforded the corresponding phenyl or phenanthrene ring fused mono-/bis-iminopyrrole ligand precursors3–8, which, upon reaction with BPh3 in an appropriate molar ratio, led to the new mono- and diboron chelate compounds Ph2 B[NC8 H5 C(H) N -2, 6-Ar] (Ar = 2, 6-iPr2 C6 H3 9 ; C6 H5 10 ), Ph2 B[(NC8 H5 C(H)N)2 -1, 4-C6 H4 ]BPh2 11, Ph2 B(NC16 H9 C(H) N -Ar) (Ar = 2, 6-iPr2 C6 H3 12 ; C6 H5 13 ), and Ph2 B[(NC16 H9 C(H)N)2 -1, 4-C6 H4 ]BPh2 14, respectively. Boron complexes12–14, containing a phenanthrene fragment fused to the pyrrolyl C3–C4 bond, are highly fluorescent in solution, with quantum efficiencies of 37%, 61% and 58% (in THF), respectively, their emission colours ranging from blue to orange depending on the extension of π-conjugation. Complexes9–11, containing a benzene fragment fused to the pyrrolyl C4–C5 bond, are much weaker emitters, exhibiting quantum efficiencies of 10%, 7% and 6%, respectively. DFT and TDDFT calculations showed that 2, 6-iPr2 C6 H3 N -substituents or, to a smaller extent, the indolyl group prevent a planar geometry of the ligand in the excited state and reveal the existence of a low energy weak band in all the indolyl complexes, which is responsible for the different optical properties. Non-doped single-layer light-emitting diodes (OLEDs) were fabricated with complexes9–14, deposited by spin coating, that of complex13 revealing a maximum luminance of 198 cd m −2 . … (more)
- Is Part Of:
- Dalton transactions. Volume 45:Issue 39(2016)
- Journal:
- Dalton transactions
- Issue:
- Volume 45:Issue 39(2016)
- Issue Display:
- Volume 45, Issue 39 (2016)
- Year:
- 2016
- Volume:
- 45
- Issue:
- 39
- Issue Sort Value:
- 2016-0045-0039-0000
- Page Start:
- 15603
- Page End:
- 15620
- Publication Date:
- 2016-09-15
- Subjects:
- Chemistry, Inorganic -- Periodicals
Chemistry, Physical and theoretical -- Periodicals
Chemistry, Inorganic -- Periodicals
546.05 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/dt#!issueid=dt043040&type=current&issnprint=1477-9226 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c6dt02771g ↗
- Languages:
- English
- ISSNs:
- 1477-9226
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3517.830000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 1381.xml