ORGANOMETALLIC COMPLEXES FOR NONLINEAR OPTICS .3. MOLECULAR QUADRATICHYPERPOLARIZABILITIES OF ENE-LINKED, IMINE-LINKED, AND AZO-LINKED RUTHENIUM SIGMA-ACETYLIDES - X-RAY CRYSTAL-STRUCTURE OF (E)-4,4'-C-CC6H4CH=CHC6H4NO2)(PPH(3))(2)(ETA-C5H5)

Citation
Ir. Whittall et al., ORGANOMETALLIC COMPLEXES FOR NONLINEAR OPTICS .3. MOLECULAR QUADRATICHYPERPOLARIZABILITIES OF ENE-LINKED, IMINE-LINKED, AND AZO-LINKED RUTHENIUM SIGMA-ACETYLIDES - X-RAY CRYSTAL-STRUCTURE OF (E)-4,4'-C-CC6H4CH=CHC6H4NO2)(PPH(3))(2)(ETA-C5H5), Organometallics, 15(7), 1996, pp. 1935-1941
Citations number
26
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
Journal title
ISSN journal
02767333
Volume
15
Issue
7
Year of publication
1996
Pages
1935 - 1941
Database
ISI
SICI code
0276-7333(1996)15:7<1935:OCFNO.>2.0.ZU;2-T
Abstract
The series of complexes E)-4,4'-C=CC(6)H(4)X=CHC6H4NO2)PR(3))(2)(eta-C 5H5) (X = CH, R = Ph, 11a; X = CH, R = Me, 11b; X = N, R = Ph, 12a; X = N, R = Me, 12b) has been synthesized by reaction of RuCl(PR(3))(2)(e ta-C5H5) with (E)-4,4'-HC=CC(6)H(4)X=CHC6H4NO2 and deprotonation of th e intermediate vinylidene complex. Complex 11a has been structurally c haracterized; it is the first example of a donor-acceptor organometall ic ''extended'' chromophore bearing the prototypical acceptor -NO2 to be crystallographically studied. Molecular quadratic hyperpolarizabili ties at 1.9 mu m were evaluated computationally for the complexes abov e and imine- and ate-linked analogues by employing ZINDO with crystall ographically obtained atomic coordinates. The results are consistent w ith a substantial increase in quadratic nonlinearity for (i) chain len gthening of the organometallic chromophore (replacing 4-C=CC6H4NO2 by (E)-4,4'-C=CC6H4CH=CHC6H4NO2) and (ii) an azo linkage compared with an ene linkage (replacing (E)-4,4'-C=CC6H4CH=CHC6H4NO2 by (E)-4,4'C=CC6H 4N=NC6H4NO2). Little variation in computed response was found upon sub stituting an imine linkage for an ene Linkage in the organometallic ch romophore (replacing (E)-4,4'-C=CC6H4CH=CHC6H4NO2 by (E)-4,4'-C=CC6H4N =CHC6H4NO2 or (E)-4,4'-C=CC6H4-CH=NC6H4NO2). Molecular quadratic optic al nonlinearities were determined experimentally for 11a, 12a, and Ru( C=CC6H4NO2-4 (PR(3))(2)(eta-C5H5) (R = Ph, Me) by electric-field-induc ed second-harmonic generation(EFISH; 11a and 12a only) and hyper-Rayle igh scattering (HRS) techniques, EFISH-derived mu beta(1064) values fo r 11a (9700 x 10(-48) cm(5) esu(-1)) and 12a (5800 x 10(-48) cm(5) esu (-1)) are large compared to those for other organometallic complexes. Resonance-enhanced quadratic nonlinearities at 1.06 mu m from HRS are large (1455 x 10(-30) cm(5) esu(-1), 11a; 840 x 10(-30) cm(5) esu(-1), 12a). Two-level-corrected values confirm a substantial increase in qu adratic nonlinearity for chain lengthening but suggest a significant d ecrease in nonlinearity on replacing an ene linkage by an imine linkag e; the latter is contrary to the ZINDO result, and the reasons for thi s are discussed.