| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1312301 | Inorganica Chimica Acta | 2013 | 9 Pages |
•Novel mono and ball-type phthalocyanines substituted with pyridine-2,6-dimethylol.•At low voltages (V <1V) all the films showed ohmic conduction.•At higher voltage (V >1V) the conduction is dominated by space charged limited conduction.•Ball type Pcs films showed an enhanced mobility ten times that of typical mono Pcs.
A new mono substituted derivatives 1 and 2 were prepared by a nucleophilic displacement reaction of 4-nitrophthalonitrile with pyridine-2,6-dimethylol. Novel metallophthalocyanines 3–4 (M = Zn, Co respectively), and ball-type binuclear phthalocyanines 5–6 with four peripheral pyridine-2,6-dimethyloxy groups were synthesized by cyclotetramerization of the phthalonitrile and characterized by elemental analyses, FT-IR, 1H NMR, UV–Vis and MALDI-TOF MS spectral data. The effects of molecular structure on the charge transport properties of novel metallophthalocyanines 3–4 and ball-type binuclear phthalocyanines 5–6 with four peripheral pyridine-2,6-dimethyloxy groups based devices are investigated using I–V measurements. From our study, we found that ball type films showed an enhanced mobility of nearly ten times that of typical mono Pcs. At low voltages (V <1V) all the films showed an ohmic conduction, whereas at higher voltage (V >1V) levels the conduction is dominated by space charged limited conduction (SCLC) with exponential distribution of trapping levels.
Graphical abstractSynthesis and characterization of novel mono and ball-type phthalocyanines with Scottky diode behavior were performed. Ball type Pcs films showed an enhanced mobility of nearly ten times that of typical mono Pcs.Figure optionsDownload full-size imageDownload as PowerPoint slide
