The photolysis of mixed ligand complexes of the type MLn(N3)2 (M=Ni, Pd, Pt; L = phosphane and diphosphane ligands, respectively; n = 1, 2) was monitored by electronic spectroscopy in absorption, emission and excitation. Initial quantum yields of these complexes were measured in CH2Cl2 and EtOH in dependence on the irradiation wavelength. Photochemically formed MOIn fragments of Pd and Pt are distinguished by an intensive emission detected at 77 K. No emission was observed with respect to the appropriate NiO fragments. An initial emission at 615 nm detected by irradiating Pd(PPh3)2(N3)2 at 77 K is explained by assuming a photochemical cis/trans isomerization Quenching experiments have been performed by using Ru(bpy)3Cl2, Os(bpy)3Cl2, Re(CO)3(phen)Cl and Cr(bpy)3(ClO4)3 as sensitizers and the mixed-ligand complexes under discussion as quenchers

Hennig, H.

Knoll, H.

Ritter, K.

Vogler, Arnd

English

University of Regensburg Publication Server

Inorganica Chimica Acta, 211 (1993) 117-120 Note 117 Spectrophotometric studies of the photolysis of diazido-bis(phosphine)-metal(I1) complexes Horst Hennig*, Klaus Ritter and Helmut Knoll Fachbereich Chemie der Universitiit Leipzig, TaktraJe 35, 04103 Leipzig (Germany) Arnd Vogler Znstitut fiir Anorganische Chemie, Universitiit Regensburg ZJniversitiitsstraJ?e 3, 93053 Regensbzq (Germany) (Received February 2, 1993; revised June 2, 1993) Abstract The photolysis of mixed ligand complexes of the type ML,,(N,), (M= Ni, Pd, Pt; L= phosphane and diphosphane ligands, respectively; n = 1,2) was monitored by electronic spectroscopy in absorption, emission and excitation. Initial quantum yields of these complexes were measured in CH,Cl, and EtOH in dependence on the irradiation wavelength. Photochemically formed MaI, fragments of Pd and Pt are distinguished by an intensive emission detected at 77 K. No emission was observed with respect to the appropriate Ni” fragments. An initial emission at 615 nm detected by irradiating Pd(PPh&(N,), at 77 K is explained by assuming a photo- chemical cis/trans isomerization. Quenching experiments have been performed by using Ru(bpy),C$, Os(bpy),Cl,, Re(CO)s(phen)C1 and Cr(bpy),(ClO& as sensitizers and the mixed-ligand complexes under discussion as quenchers. Electron-rich metal complex fragments of low-valent platinum, palladium and nickel with phosphine as sta- bilizing ligands are of considerable catalytic interest, particularly when the activation of small molecules is regarded. Such metal(O) fragments may be generated photochemically (eqn. (1)) and can be used as catalysts [l] in particular with respect to the catalytic activation of acetylene and alkyne derivatives [2]. M”(N&L 2 M”L + 3N, (I) The general photochemical behaviour of mixed-ligand azido complexes of nickel(II), palladium(I1) and plat- *Author to whom correspondence should be addressed. 0020-1693/93/$6.00 inum(I1) has been summarized very recently [3]. A few results are published on the photochemistry of the starting M(N&L complexes [4-71 and only little is known regarding the luminescence spectroscopic prop- erties of the corresponding metal(O) fragments. Thus, it has been shown that Pt(PPh,), exhibits a blue emission at 77 K [4, 91. Within the framework of our investigations in photocatalysis [8] we were interested in further details of the photolysis of mixed-ligand complexes of the sort M(N&L [lo] and in particular in the spectroscopic properties of their metal(O) fragments ML, (M= Pt, Pd, Ni; I+= dppe, dppp; L= PPh3 where dppe = l,Zbis(diphenyl- phosphino)ethane, dppp = 1,3-bis(diphenylphosphino)- propane). In addition to our earlier results [2, 4-71 we want to report on the stationary photolysis of M(N,)L, complexes at room temperature as a functio3of the irradiation wavelength, the emission and excitation spec- tra of the photochemically generated and catalytically active metal(O) fragments ML, and the evaluation of the photolysis of Pd(N,),(PPh,), at 77 K by emission end excitation spectroscopy. Finally, some preliminary results of the quenching of Ru(bpy),Cl, and other sensitizers in the presence of M(N,)L, mixed-ligand complexes will be reported. The M(N,)L, mixed-ligand complexes were prepared according to the literature [ll-141. Solutions in CH,Cl,, THF, 2-MeTHF or ethanol were used for the photolysis experiments. The solvents were distilled and dried according to standard procedures. All solutions were purged with argon before using. Luminescence spectra were obtained by using a Perkin-Elmer LS50 spectro- photometer with a 10 ps pulsed 200 W xenon lamp. The low temperature studies were performed in a quartz tube cuvette in a cryostat adapted to the IS50 and cooled by liquid nitrogen. A 200 Hg-Xe lamp model LTi02-A102S (AMKO LTI, wissenschaftlich-technische Instrumente GmbH) in vertical position was used as irradiation source for irradiation of samples within the quartz tube cuvette positioned in the cryostat. The absorption spectra of the mixed-ligand azido complexes can be divided into areas distinguished by d-d transitions ( > 350 nm), azide-to-metal (250-330 nm) and metal-to-phosphine ( < 250 nm) charge-transfer transitions. The following results were obtained with respect to the stationary photolysis as a function of the irradiation wavelength. Table 1 summarizes the initial photolysis quantum yields in dependence on the irradiation wavelength when using CH,Cl, as solvent. 0 1993 - Elsevier Sequoia. All rights reserved 118 TABLE 1. Initial photolysis quantum yields in dependence on the irradiation wavelength in CH2C12 at room temperature 254 nm 313 nm (LM(JT) (LMCT) 365 nm (d-d) W’PhMV2 0.007 f 0.01 0.10 *0.01 0.095 f 0.01 Pd(PPhMN& 0.06 f 0.005 0.022 f 0.005 Ni(dppp)(N& 0.7 + 0.005 0.014 f 0.005 GO 320 360 400 440 400 Wavelength, nm Fig. 1. Luminescence spectra of Pt(PPh,), (-), Pt(dppp) (- --) and Pt(dppe) (. . . .) in ethanol at 77 K after photolysis of Pt(N,),L, (L = PPh,, I+ = dppp and dppe; emission bold, excitation thin). The quantum yields of nickel and palladium complexes decrease with increasing irradiation wavelength. How- ever, no significant dependence was observed in the case of the platinum complexes. Upon irradiation with visible light (A,,<350 nm) the LMCT band disappears due to the oxidation of the azide ligands. Coupling of d-d and LMCT excited states seems to be responsible for that behaviour which is assumed to play no role in the case of palladium and nickel complexes. That conclusion is in agreement with the increasing ligand field splitting with increasing atomic number within a transition-metal group. Upon irradiation of the platinum(I1) and palla- dium(I1) mixed-ligand complexes in ethanol (c G lop3 mol l-l, Ai,> 250 nm) at 77 K, emission has been observed that originates unambiguously from the cor- responding M”L, fragments. Figure 1 shows the un- corrected electronic emission and excitation spectra of Pt’L. The emission spectra are distinguished by a band maximum at 445 nm and the excitation spectra exhibit two bands around 330 and 400 nm, each of them with a shoulder at the high energy side. An usual band separation procedure applied to the spectra of Pt(PPh,), yields band maxima at 322, 340, 392 and 400 nm. The excitation spectrum of Pt(PPh,), at 77 K in ethanol is in excellent agreement with the difference absorption spectrum in benzene at room temperature after laser 260 300 340 380 420 460 500 Wavelength, nm Fig. 2. Luminescence spectra of Pd(PPh,), (-) and Pd(dppp) (-- -) in ethanol after photolysis of Pd(N,),(PPh,), and Pd(N,),(dppp) at 77 K (emission bold, excitation thin). flash photolysis of Pt(O,)(PPh,),. In this case the photolysis led also to the formation of Pt(PPh,), [9]. Interestingly, there are no significant differences in the luminescence spectra of di- or monodendately co- ordinated phosphine ligands as shown in Fig. 1, whereas the luminescence intensity is decreased in the order Pt(PPh,), > Pt(dppp) > Pt(dppe). After irradiation of Pd(N,),(PPh,), and Pd(N,),- (dppp) in ethanol at 77 K with wavelengths Ai,& 260 nm an emission band at 437 nm was observed. The excitation spectra show a maximum at 375 nm and a shoulder around 300 nm (Fig. 2). We assign these spectra to Pd(PPh,), and Pd(dppp), respectively. The emission disappears upon warming up to room temperature where formation of the dimer M,(L), species is expected. Contrary to the platinum and palladium mixed-ligand complexes no luminescence was observed during the photolysis of Ni(N,),(dppe) and Ni(N,),(dppp) at 77 K. This is in agreement with the decreasing of the luminescence intensities of PdL, when compared with PtI+ In ethanol, MeTHF or in the solid state the starting complex Pd(N3)2(PPh3)2 exhibits at low temperature (77 K) an intense red emission at 615 nm (Fig. 3). A luminescence lifetime of 74 Ifr 1.5 ps has been estimated. The excitation spectrum shows bands around 400 nm. The relatively long lifetime and the weak absorption bands at 400 and 470 nm (E< 1) in ethanol refer to a spin-forbidden phosphorescence transition. The emission at 615 nm disappears upon excitation of the complex at 400 nm leading to the expected emission of Pd(PPh,), at 437 nm as shown in Fig. 4. It can be clearly seen from Fig. 4 that there is a fast decrease of the emission of Pd(N3)2(PPh3), (615 nm) and a delayed appearance of the luminescence of Pd(PPh,), (437 nm) indicating a non-luminescence spe- cies obviously due to the formation of an intermediate isomerization product [7, 151. 119 lntenslt” I ’ ,I 300 I’ ‘, ,--’ I I I ; : -\ I I\ ’ 200 /‘\\,I 100 I ^I’ \ I _ :‘:\\\ \ \ \ 1 \ \ \ 0 /, > 1 230 260 330 360 430 460 530 560 630 660 Wavelength, nm Fig. 3. Luminescence spectra of Pd(N&(PPh& in 2-MeTHF at 77 K (---, excitation; -, emission). t 250 A 50 0 400 450 500 550 600 650 700 Wavelength, nm Fig. 4. Change of the luminescence spectra upon irradiation of Pd(N&(PPh& in 2-MeTHF at 77 K (starting with the spec- trometer light source at A,, = 400 nm and continuing with A,, > 300 nm of an Hg-lamp to accomplish the formation of Pd(PPh,), emitting at 437 nm). Because the bidentate ligands dppe and dppp nec- essarily form cfi-Pd(N,),L, complexes and do not show any emission around 600 nm, we assign the emission band of Pd(N,),(PPh,), at 615 nm to the puns-isomer. The following two separate primary photolysis steps can therefore be assumed (eqns. (2) and (3)). puns-Pd(N,),(PPh,), 5 &Pd(N,),(PPh,), (2) cis-Pd(N,),(PPh3)z -% cti-Pd(PPh,), + 3N, t (3) Preliminary experiments have shown that the emission of Ru(bpy),Cl, at 600 nm is quenched by the mixed- ligand azido complexes under discussion in CH,Cl, solution at room temperature. The quenching rate constants determined by means of Stem-Volmer plots and their dependence on different phosphine ligands can be explained by assuming a diffusion controlled luminescence quenching (Table 2). With the increasing size of the phosphine ligands the rate constants decrease. Further, we have been able TABLE 2. Rate constants for the luminescence quenching of Ru(bpy),Cl, in CHrClr, k ( lo9 M s-‘) (I\.Xcita,iOn =460 nm, hemirrion = 615 nm; the relative ratio between luminescence inten- sities (la/r,) was corrected with respect to the inner filter effect WI) L= PPh3 L2 = dppp L2 = dppe PtWW, 3.1*0.3 5.1*0.1 10.8 f 0.5 PdL2(N& 26.1+ 1 29.4+2 90*5 NiL2(N& 11.8+0.1 19.3+0.8 to show that the triplet emission of Os(bpy),Cl, [17] and Re(CO),(phen)Cl [18, 191 is also quenched by the mixed-ligand azido complexes within the diffusion con- trolled limit. However, the doublet emission of Cr(bipyMClO& PO1 was not quenched. This result suggests that triplet acceptor orbitals might by involved in those complexes which are efficiently quenched. The palladium complexes exhibit larger quenching rate constants as compared with the corresponding platinum or nickel complexes. However, it cannot yet be decided whether electron transfer or energy transfer quenching is operative. This question is currently under investigation. Acknowledgement The financial support of this project by the ‘Deutsche Forschungsgemeinschaft’ is gratefully acknowledged. References 1 2 9 10 11 12 13 W.C. Trogler, in A.B.P. Lever (ed.), Excited State and Reactive Intermediates, ACS Symposium Series 307, American Chemical Society, Washington, DC, 1986, p. 177. H. Hennig, L. Weber and D. Rehorek, in C. Kutal (ed.), Photosensitive Metal-Organic Systems, American Chemical So- ciety, Washington, DC, in press. H. Hennig, R. Stich, H. Knoll, D. Rehorek and D.J. Stufkens, Coord. Chem. Rev., 111 (1992) 131. A. Vogler, R.E. Wright and H. Kunkely, Anger. Chem., 92 (1980) 745. H. Hennig, R. Stich, D. Rehorek, P. Thomas and T.J. Kemp, Znorg. Chim. Acta, 143 (1988) 7. H. Hennig, R. Stich, H. Knoll and D. Rehorek, Z. Anorg Allg. Chem., 567 (1989) 139. H. Knoll, R. Stich, H. Hennig and D.J. Stufkens, Znorg. Chim. Acta, 178 (1990) 71. H. Hennig, L. Weber, R. Stich, M. Grosche and D. Rehorek, in J.F. Rabek (ed.), Progress in Photochemistry and Photophysics, Vol. VI, CRC, Boca Raton, FL, 1992, p. 167. S. Oishi and K. Suzuki, Chem. Lett., (1991) 171. K. Ritter, Diploma thesis, University of Leipzig, Leipzig, 1992. A.D. Westland, J. Chem. Sot., (1965) 3060. W. Beck, W.P. Fehlhammer, P. Pollemann, E. Schuierer and K. Feldl, Chem. Ber., 100 (1967) 2357. K. Bowmann and Z. Dori, Znorg Chem., 9 (1970) 395. 120 14 P.H. Kreutzer, K.T. Schorpp and W. Beck, 2. Naturforsch., 17 D.E. La&y, B.J. Pankuch and G.A. Crosby, J. Phys. Chem., 30 (1975) 544. 84 (1980) 2068. 15 D.A. Redfield, L.W. Gary and J.H. Nelson, Inorg. Chem., 14 18 G.L. Goffroy and M.S. Wrighton, Organornefallic Photochem- (1975) 50. &try, Academic Press, New York, 1979. 16 D. Rehorek, A. Rehorek, A. Ackermann, P. Thomas and H. 19 A.J. Lees, C/rem. Rev., 87 (1987) 711. Hennig, J. Inform. Rec. Mater., (1981) 291. 20 A.D. Kirk and G.P. Porter, J. Phys. Chem., 84 (1980) 887. 

Spectrophotometric studies of the photolysis of diazido-bis(phosphine)-metal(II) complexes

http://epub.uni-regensburg.de/13570/1/vogler92.pdf

Spectrophotometric studies of the photolysis of diazido-bis(phosphine)-metal(II) complexes

Abstract

Similar works

Full text

Available Versions

University of Regensburg Publication Server

University of Regensburg Publication Server