Synthesis and spectroscopic characterization of Ni, Zn, Pd and Pt tetra(pentafluorophenyl)porpholactone with comparisons to Mg, Zn, Y, Pd and Pt metal complexes of tetra(pentafluorophenyl)porphine

2002 ◽  
Vol 06 (02) ◽  
pp. 135-145 ◽  
Author(s):  
Gamal Khalil ◽  
Martin Gouterman ◽  
Stephen Ching ◽  
Colin Costin ◽  
Lisa Coyle ◽  
...  

Ni , Zn , Pd and Pt tetra(pentafluorophenyl)porpholactone (TFPL) were synthesized and identified by their optical and mass spectra. The lactone ring was produced from the parent free-base porphyrin using silver nitrate and oxalic acid with a yield of 73%, and the metals were inserted by standard procedures from metal salts. The compounds show intense Soret Bands in the region 390-420 nm. The longest wavelength visible absorbance peaks, in the region 572-608 nm, are weaker than the Soret peaks by a factor of only ~3 for the Ni , Pd , and Pt complexes but a factor of ~10 for the free-base and Zn complexes. As found with other metalloporphyrins the Ni complex is dark, Zn shows fluorescence and Pd and Pt complexes show strong phosphorescence. The Pd complex also shows a weak fluorescence not quenched by oxygen. The phosphorescence lifetimes of Pd and Pt complexes of TFPL in 3-methylpentane at 77 K are, respectively, ~1 ms and ~70 μs, about 60% that of the TFPP complexes. The wavelengths of phosphorescence emission, 733 nm and 758 nm for PtTFPL and PdTFPL, respectively, are sufficiently red-shifted so that these pressure sensitive luminophors can be included in the same pressure sensitive paint (PSP) as Eu complexes, whose emission at ~615 nm can serve as a temperature sensor. The fluorescences of Mg , Zn , and Y(TFPP) show weak origin bands, making them suitable as unquenched references for PSP.

1986 ◽  
Vol 41 (8) ◽  
pp. 971-973 ◽  
Author(s):  
Hartmut Köpf ◽  
Thomas Klapötke

Abstract Bis(/75-cyclopentadienyl)-chloro-selenophenolatotitanium (IV), Bis(?75-cyclopentadienyl)-chloro-selenophenolatozirconium (IV), Bis(//5-cyclopentadienyl)-chloro-selenophenolatohafnium (IV), Bis(^5-cyclopentadienyl)-chloro-selenophenolatotungsten(IV), Mass Spectra The metallocene chloro selenophenolates C p;M Cl(SeChH 5) (Cp = ^5-C5H 5; M = Ti, Z r, Hf, W) were prepared by reaction of Cp2MCl2 with equivalent am ounts of LiSeC6H 5, obtained from phenylselenol and «-butyllithium, and were characterized by 'H NM R, IR and MS data. The fragmentation behaviour of the Ti and W derivatives is elucidated by observing m etastable transi­ tions in the mass spectra.


2017 ◽  
Vol 21 (10) ◽  
pp. 680-691
Author(s):  
Kaarin K. Evens ◽  
Kathryn E. Splan

The addition of arylethynyl groups to the porphyrin macrocycle represents an effective strategy with which to enhance the light-harvesting properties of porphyrins. We now extend this modification to arylethynyl porphyrins with two or four [Formula: see text]-hydroxyphenyl substituents. Arylethynyl porphyrins bearing four, but not two, [Formula: see text]-hydroxyphenyl substituents show evidence of aggregation under acidic conditions. Under basic conditions, deprotonation of the peripheral hydroxyphenyl substituents results in substantially red-shifted spectral features and enhanced absorption in the Q-band region. When the hydroxyphenyl groups are appended to the porphyrin macrocylce via the ethynyl spacers, the spectral shifts observed upon deprotonation are significantly enhanced relative to those observed for hydroxyphenylporphyrins, highlighting the role of expanded conjugation in altering porphyrin photophysics.


2014 ◽  
Vol 2014 ◽  
pp. 1-7
Author(s):  
Gauri D. Bajju ◽  
Altaf Ahmed ◽  
Deepmala Gupta ◽  
Ashu Kapahi ◽  
Gita Devi

The synthesis and spectroscopic characterization of new axially ligated indium(III) porphyrin complexes were reported. Chloroindium(III) porphyrin (TPPIn-Cl) was obtained in good yield by treating the corresponding free base with indium trichloride. The action of the different phenols on chloroderivatives (TPPIn-Cl) led to the corresponding phenolato complexes (TPPIn-X). These derivatives were characterized on the basis of mass spectrometry,1H-NMR, IR, and UV-visible data. The separation and isolation of these derivatives have been achieved through chromatography. The spectral properties of free base porphyrin and its corresponding metallated and axially ligated indium(III) porphyrin compounds were compared with each other. A detailed analysis of UV-Vis,1H-NMR, and IR suggested the transformation from free base porphyrin to indium(III) porphyrin. Besides,13C-NMR and fluorescence spectra were also reported and interpreted. The stability of these derivatives has also been studied through thermogravimetry. The complexes were also screened for anticancerous activities. Among all the complexes, 4-MePhO-InTPP shows highest anticancerous activity. The title complexe, TPPIn-X (where X = different phenolates), represents a five-coordinate indium(III) porphyrin complex in a square-pyramidal geometry with the phenolate anion as the axial ligand.


2005 ◽  
Vol 58 (7) ◽  
pp. 517 ◽  
Author(s):  
Yannick Teral ◽  
Gabriel Roubaud ◽  
Claude Aubert ◽  
Robert Faure ◽  
Mylène Campredon

The synthesis of some new fluoro-2H-1-benzopyran derivatives utilizing a reaction between titanium phenolates and β-phenylcinnamaldehydes in toluene is reported. These compounds were characterized by NMR and UV/visible spectroscopy as well as mass spectrometry. In solution all the compounds are photochromic. Complete assignment of the 1H and 13C resonances was achieved by concerted application of homonuclear (gs-COSY), proton-detected (C, H) one-bond (gs-HMQC), and long-range (gs-HMBC) heteronuclear two-dimensional chemical shift correlation experiments using a 500 MHz NMR spectrometer equipped with a cryoplatform and a 5 mm cryoprobe. The mass spectra of the different compounds were characterized by intense molecular and high fragment ions. The introduction of an atom of fluorine as a molecular probe is of interest in determining the mechanistic aspects of the photochemical process.


2012 ◽  
Vol 53 (6) ◽  
pp. 1737-1749 ◽  
Author(s):  
Martin Bitter ◽  
Tatsuya Hara ◽  
Rainer Hain ◽  
Daisuke Yorita ◽  
Keisuke Asai ◽  
...  

1985 ◽  
Vol 40 (9) ◽  
pp. 1134-1138 ◽  
Author(s):  
H. G. Alt ◽  
H. E. Engelhardt

The photo-induced reaction of CpV(CO)4 (1) (Cp =η5-C5H5) with alkynes R1C2R2 (R1, R2 = H, Me, Ph, SiMe3) in pentane solution yields the substitution products CpV(CO)2R1C2R2 (2). One CO ligand of complexes 2 is readily displaced by PMe3 or tBuNC affording the derivatives CpV(CO)(L)R1C2R2 {3(PMe3), 4 (tBuNC)}. Compounds 2-4 are characterized by their IR, 1H, 13C, 51V NMR and mass spectra. The alkyne in compounds 2-4 shows typical features of a four electron ligand. The barrier for the rotation of the alkyne ligand around the vanadium alkyne bond axis in the complexes 3-4 is comparatively low (⊿ G≠ = 44.4-68.3 kJ/mol) depending mainly on the steric requirements of the acetylene ligand.


1994 ◽  
Vol 49 (1) ◽  
pp. 119-127 ◽  
Author(s):  
Anne-Kathrin Duhme ◽  
Henry Strasdeit

Abstract In toluene, bis(pentafluorophenyl)cadmium(II) and thiols RSH (R = But, 2,4,6-Pri3C6H2, 2,4,6-But3C6H2) react to give soluble pentafluorophenyl cadmium thiolates [(Cd(C6F5)(SR)}n] The compounds [{Cd(C6F5)(SBut)}4] (1) ∙ 0.5 C6H5CH3, [ {Cd(C6F5)(SC6H2Pri3-2,4,6)}n ] (2) ∙ ca. 0.25n C6H5CH3, and [{Cd(C6F5)(SC6H2But3-2,4,6)} n] (3) ∙ ca. 0.25 n C6H5CH3 have been prepared in 65, 59 and 78% yield, respectively. 1 ∙ 0.5 C6H5CH3 crystallizes in the triclinic space group P1̄ with a = 11,635(1)Å, b = 11.583(1)Å, c = 21.480(2)Å, α = 82.12(1)°, β = 76.26(1)°, γ = 89.35(1)°, and Z = 2. 1 is a cubane-type complex with a {Cd4(μ3-SBut)4}4+ core. Each Cd atom is coordinated by three bridging thiolato ligands and one terminal C6F5 group (Cd - S 2.62 Å, Cd - C 2.15 Å (mean values)). The central C atoms of the ButS− ligands of 1 show a remarkable low-field shift o f their 13C NMR resonance (12.3 ppm relative to the value of the free thiol). A characteristic spectral feature of (Cd(C6F5) }+ complexes is the large value of the coupling constant 2J (19F ,13C) of the ipso-C atom (1, 2: 68 Hz; 3: 67 Hz). The complexes [Cd(C6F5)(SR) + H]+, [Cd(SR)2 + H]+, and [Cd2(SR)3]+ were identified in the Cl mass spectra (iso-butane) of 2 and 3.


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