The anisotropy of the triplet sublevel populating rates was determined for 1 , 1 0-phenanthroline ( phen), 2,9dimethyl-1,l Ophenanthroline (2,9-Me2phen) and their zinc(H) complexes in rigid solutions and for ZnClz(2,9-Merphen) in the crystalline state at 77 K by a time-resolved EPR technique. The su
Complex formation of ruthenium(IV) and osmium(VIII) with 1,10-phenanthroline on the surface of silica sorbents
✍ Scribed by T.I. Tikhomirova; V.I. Fadeeva; G.V. Kudryavtsev
- Publisher
- Elsevier Science
- Year
- 1992
- Tongue
- English
- Weight
- 625 KB
- Volume
- 257
- Category
- Article
- ISSN
- 0003-2670
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✦ Synopsis
A study was made of the sorption of ruthemum(IV) and osrmum(VIII) by sdlca and slhca with chemically grafted sulpho groups from solutions containing l,lO-phenanthrohne Usmg diffuse reflection, lummescence and x-ray photoelectron spectroscopic methods, it was found that durmg sorption at pH 6-7 and room temperature on the surface of silica sorbcnts phenanthrohnate complexes of various composition are formed, bls-and tns(l,lOphenanthrohne)metal (II, III), the Os(II) to O&II) mole ratlo bemg 2 1 A quantltatwe yield of tr&l,lOphenanthrolme)metal(II) complex IS obtamed at 98 f 2' C The rate of complex formation on the surface of the sorbents consIderably exceeds the rate of formatlon of the corresponding complexes m solution It P suggested that slhca sorbents have a catalytic action on the process of formation of complexes of ruthenium and osmmm with l,lO-phenanthrohne on the sorbent surface A rapId sorption-lummescenc method for determmmg ruthemum and osmmm IS proposed The detectlon lumt is 7 X 10e4 /Lg ml-' for ruthemum and 1 X 10e3 pg ml-' for osmnun
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C Chemical shifts are reported for the ruthenium(II) tris complexes of thirteen 2,Z-bipyridyls and three 1,lO-phenanthrolines and for the osmium(]") bris complexes of five 2,2'-bpyridyls. Chelation induced shifts -&3 are discussed in terms of models for n back-bonding. -C NMR is shown to be a conven
Surface-enhanced resonance Raman spectra @ERRS) of the complexes PAPH-Co(II), PAPH-Ni(II), PAPH-Fe(II), and PHEN-Fe(I1) (PAPH = 2-pyridine carboxyaldehyde 2-pyridylhydrazone and PHEN = l,lO-phenanthroline) adsorbed on silver colloid have been studied. Differences among SERS spectra of ligands and SE
Dynamics of ternary complex formation in the reaction of diaquoanthranilato-N , Ndiacetatonickelate(l1) with 2,2'-bipyridine and I ,lo-phenanthroline. Ni(adal( H2012- ## and L = bipy or phen The kinetics of formation of ternary complexes by diaquoanthranilato-N, Ndtacetatonickelate[ i l ) , [Nl(a
## Abstract A novel ligand 3‐(1__H__‐imidazo[4,5‐__f__][1,10]phenanthrolin‐2‐yl)‐4__H__‐1‐benzopyran‐4‐one (ipbp) and its ruthenium(II) complexes [Ru(bpy)~2~(ipbp)]^2+^ (**1**) and [Ru(ipbp)(phen)~2~]^2+^ (**2**) (bpy=2,2′‐bipyridine, phen=1,10‐phenanthroline) were synthesized and characterized by
## Abstract The new ligand bdip (=2‐(1,3‐benzodioxol‐4‐yl)‐1__H__‐imidazo[4,5‐__f__][1,10]phenanthroline) and its Ru^II^ complexes [Ru(4,7‐dmp)~2~(bdip)]^2+^ (**1**; 4,7‐dmp=4,7‐dimethyl‐1,10‐phenanthroline) and [Ru(bpy)~2~(bdip)]^2+^ (**2**; bpy=2,2′‐bipyridine) were synthesized and characterized