1518-61-2 Purity
95%
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Specification
This work describes a method for preparing transition metal complexes of tin(II) phthalocyanine (SnIIPc) in the neutral, monoanionic, and dianionic states, taking advantage of the ability of tin atoms to form stable Sn-M bonds with transition metals (Mo, Fe, Rh, and Ru). This method can be used to develop magnetic and conductive components based on metal phthalocyanines and transition metals.
· Key Conclusions
Except for CpFe(CO)2, the negative charge and spin of the coordinated [SnIIPc(3-)]·- radical anions were maintained, allowing these anions to function as anionic paramagnetic ligands for the transition metals. In the coordination complex formed between CpFeI(CO)2 and [SnIIPc(3-)]·- (4), an unusual charge transfer occurred, resulting in the generation of {CpFeII(CO)2}+ cations and [SnIIPc(4-)]2- dianions. Additionally, it was discovered that the formally neutral Ph5CpRuII(CO)2[SnIIPc] molecule contains [SnIIPc(3-)]·- radical anions, making it particularly noteworthy due to its exhibiting strong magnetic spin coupling.
· Synthesis Case
The compound {Cryptand(Na+)}[SnIIPc(3-)]·-·C6H4Cl2 (3) was synthesized by reducing SnIIPc (26.4 mg, 0.042 mmol) with a slight excess of sodium fluorenone ketyl (11 mg, 0.054 mmol) in the presence of 1 equivalent of cryptand (16 mg, 0.042 mmol) in o-dichlorobenzene (16 mL) at 100 °C for 2 hours. After cooling the resulting deep blue solution to room temperature, it was filtered into a tube for diffusion. This process yielded black parallelepiped crystals of 3, exhibiting a distinctive copper luster, with a 74% yield.
Organic solar cells (OSCs) based on tin(II) phthalocyanine (SnPc)/C60 heterojunction were prepared, and the effect of SnPc thickness on the device electrical characteristics was studied. According to the results, power conversion efficiency was 0.79% with SnPc thickness of 15 nm which has the highest JSC and highest VOC, with tolerable FF.
Preparation of OPV cells
· The OPV cells tested were OPV cells ITO/PEDOT:PSS (10 nm)/MoO3 (10 nm)/SnPc (x nm)/C60 (40 nm)/BPhen (10 nm)/Ag, with x equal to 6, 9, 12, 15, and 18. The devices were manufactured on indium-tin oxide (ITO) coated glass substrates with 180 nm thickness and sheet resistance of 10 /sq.
· Prior to loading into a vacuum chamber, the ITO substrates were thoroughly cleaned in ultrasonic baths with detergent, acetone, ethanol, and deionized water for 10 minutes each, followed by drying with high-purity nitrogen. The substrates underwent an O2 plasma treatment for 5 minutes before being coated with PEDOT:PSS by spin-coating.
· After this, layers of MoO3, SnPc, C60 and BPhen were followed by sequential evaporates on to the ITO substrates using an OLED-V organic multifunctional vacuum deposition system at 1-2 Å/s and 3×10^-4 Pa. Then silver was vaporised, as the cathode, at about 10 /s, at 3×10^-3 Pa.
The molecular formula is C32H16N8Sn.
The synonyms are Phthalocyanine Tin(II), 2,11,20,29,37,38-Hexaza-39,40-diazanidanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13,15,17,19,21(38),22,24,26,28,30(37),31,33,35-nonadecaene;tin(2+), [Phthalocyaninato(2-)]tin, DTXSID00424848, and tin(2+) phthalocyanine-29,31-diide.
The molecular weight is 631.2 g/mol.
The parent compound is Phthalocyanine.
The component compounds are Phthalocyanine, Tin powder, and 31h-Phthalocyanine.
It was created on May 3, 2006.
It was last modified on October 21, 2023.
The IUPAC name is 2,11,20,29,37,39-hexaza-38,40-diazanidanonacyclo[28.6.1.13,10.112,19.121,28.04,9.013,18.022,27.031,36]tetraconta-1,3,5,7,9,11,13,15,17,19(39),20,22,24,26,28,30(37),31,33,35-nonadecaene;tin(2+).
The InChI is InChI=1S/C32H16N8.Sn/c1-2-10-18-17(9-1)25-33-26(18)38-28-21-13-5-6-14-22(21)30(35-28)40-32-24-16-8-7-15-23(24)31(36-32)39-29-20-12-4-3-11-19(20)27(34-29)37-25;/h1-16H;/q-2;+2.
The CAS number is 15304-57-1.