inalladsorptionsteps,andthreewaterwashingstepsfor1minwereperformed after deposition of each layer. Subsequent (PEI/PSS/PAH/PSS)/Au NP layers were deposited in identical fashion. The same procedure and conditions were usedforthedepositionofthePE/CdTeNPlayers,withtheexceptionthatPEI/ PSS/PAHinterlayerswereusedbetweeneachCdTeNPlayer.Thatis,theCdTe NPswereadsorbedinalternationwithPAH/PSS/PAHforpreparing(PE 3 /CdTe NP) 3 and (PE 3 /CdTe NP) 6 samples. As for the PE NTs, the top and bottom coatingsonthePCmembraneswerewipedawaywithfilterpaper.Thecompos- iteNTswerethenreleasedbydissolvingthePCmembraneindichloromethane, andtheNTdispersionsobtainedwerefinallypurifiedbyseveraldichlorometh- anewashingsandcentrifugationcycles,followedbyredispersioninwater. Characterization: SEM images were recorded with a JEOL (JSEM 6330 F) instrument operated at an acceleration voltage of 5 kV. SEM samples were sputter-coated with Pt. TEM and EDX measurements were performed with a PhilipsCM12microscopeoperatedat120kV.SamplesforTEMandEDXwere suspended in water by applying ultrasound, and then an aliquot of the suspen- sion was pipetted onto carbon-coated copper grids. UV-vis spectra were re- cordedusingaCary4Espectrophotometerequippedwithadiffusereflectance attachment. Fluorescence spectra were obtained using a Spex Fluorolog-2 (model FL-2T2) spectrofluorimeter. An excitation wavelength of 380 nm was used. Confocal microscopy images were taken with a Leica TCS SP equipped with100oilimmersionobjective. Received:June23,2003 Finalversion:August19,2003 Publishedonline:October10,2003 ± [1] a) S. Iijima, Nature 1991, 354, 56. b) M. S. Gudiksen, L. J. Lauhon, J.Wang,D.C.Smith,C.M.Lieber, Nature 2002, 415,617.c)A.Bachtold, P.Hadley,T.Nakanishi,C.Dekker, Science 2001, 294,1317. [2] G.R. Patzke, F. Krumeich, R. Nesper, Angew. Chem. Int. Ed. 2002, 41, 2446. [3] C.N.R.Rao,M.Nath, Dalton Trans. 2003, 1,1. [4] C. R.Martin, Science 1994, 266,1961. [5] N. I.Kovtyukhova,T. E.Mallouk, Chem. Eur. J. 2002, 8,4355. [6] S.R. Nicewarner-Pena, R. G. Freeman, B. D. Reiss, L. He, D. J. Pena, I. D. Walton, R. Cromer, C. D. Keating, M. J. Natan, Science 2001, 294, 137. [7] G. Sauer, G. Brehm, S. Schneider, K. Nielsch, R. B. Wehrspohn, J. Choi, H.Hofmeister,U.Gösele, J. Appl. Phys. 2002, 91,3243. [8] M. Steinhart, J. H. Wendorff, A. Greiner, R. B. Wehrspohn, K. Nielsch, J.Schilling,J.Choi,U.Gosele, Science 2002, 296,1997. [9] M.Nishizawa,V.P.Menon,C.R.Martin, Science 1995, 268,700. [10] B.B.Lakshmi,C.J.Patrissi,C.R.Martin, Chem. Mater. 1997, 9,2544. [11] S.J.Limmer,S.Seraji,Y.Wu,T.P.Chou,C.Nguyen,G.Cao, Adv. Funct. Mater. 2002, 12,59. [12] D. Routkevitch, T. Bigioni, M. Moskovits, J. M. Xu, J. Phys. Chem. 1996, 100,14037. [13] X. Y. Zhang, L. D. Zhang, G. W. Meng, G.H. Li, N. Y. Jin-Phillipp, F.Phillipp, Adv. Mater. 2001, 13,1238. [14] H.Q.Cao,Y.Xu,J.M.Hong,H.B.Liu,G.Yin,B.L.Li,C.Y.Tie,Z.Xu, Adv. Mater. 2001, 13,1393. [15] M. S. Sander, A. L. Prieto, R. Gronsky, T. Sander, A. M. Stacy, Adv. Mater. 2002, 14,665. [16] V.M.Cepak,C.R.Martin, Chem. Mater. 1999, 11,1363. [17] W.Lee,J.Lee, Adv. Mater. 2002, 14,1187. [18] G. Che, B. B. Lakshmi, C. R. Martin, E.R. Fisher, Langmuir 1999, 15, 750. [19] G.Che,E.R.Fisher,C.R.Martin, Nature 1998, 393,346. [20] T.Kyotani,L.F.Tasi,A.Tomita, Chem. Commun. 1997,701. [21] J.Luo,L.Zhang,Y.Zhang,J.Zhu, Adv. Mater. 2002, 14,1413. [22] G.Decher,J.D.Hong, Ber. Bunsen-Ges. 1991, 95,1430. [23] G.Decher, Science 1997, 277,1232. [24] A. A. Mamedov, A. Belov, M. Giersig, N. N. Mamedova, N.A. Kotov, J. Am. Chem. Soc. 2001, 123,7738. [25] a) C. Tedeschi, F. Caruso, H. Möhwald, S. Kirstein, J. Am. Chem. Soc. 2000, 122,5841.b)W.Jin,X.Shi,F.Caruso, J. Am. Chem. Soc. 2001, 123, 8121. [26] a) F. Caruso, R. A. Caruso, H. Möhwald, Science 1998, 282, 1111. b) E. Donath, G. B. Sukhorukov, F. Caruso, S. A. Davis, H. Möhwald, Angew. Chem. Int. Ed. 1998, 37, 2201. c) F. Caruso, H. Lichtenfeld, E. Donath, H.Möhwald, Macromolecules 1999, 32,2317. [27] For reviews, see: a)F. Caruso, Adv. Mater. 2001, 13, 11. b) F. Caruso, Chem. Eur. J. 2000, 6,413. [28] D. I. Gittins, A.S. Susha, B. Schoeler, F. Caruso, Adv. Mater. 2002, 14, 508. [29] Z.Liang,A.S.Susha,F.Caruso, Adv. Mater. 2002, 14,1160. [30] A. Rogach, A. Susha, F. Caruso, G. Sukhorukov, A. Kornowski, S. Ker- shaw,H.Möhwald,A.Eychmüller,H.Weller, Adv. Mater. 2000, 12,333. [31] K.S.Mayya,D.I.Gittins,A.M.Dibaj,F.Caruso, Nano Lett. 2001, 1,727. [32] D.Wang,F.Caruso, Chem. Commun. 2001,489. [33] a) J. J. Harris, J. L. Stair, M.L. Bruening, Chem. Mater. 2000, 12, 1941. b) A. M. Balachandra, J. Dai, M. L. Bruening, Macromolecules 2002, 35, 3171. [34] S.Y.Nam,Y.M.Lee, J. Membr. Sci. 1997, 135,161. [35] F.v.Ackern,L.Krasemann,B.Tieke, Thin Solid Films 1998, 327,762. [36] N.A.Kotov,S.Maganov,E.Tropsha, Chem. Mater. 1998, 10,886. [37] P. Stroeve, V. Vasquez, M.A. N. Coehlo, J. F. Rabolt, Thin Solid Films 1996, 284,708. [38] J.-M.Leväsalmi,T. J.McCarthy, Macromolecules 1997, 30,1752. [39] P.Schuetz,F.Caruso, Adv. Funct. Mater.,inpress. [40] D.I.Gittins,F.Caruso, Angew. Chem. Int. Ed. 2001, 40,3001. [41] a) A. L. Rogach, L. Katsikas, A. Kornowski, D. Su, A. Eychmuller, H.Weller, Ber. Bunsen-Ges. 1996, 100,1772.b)N.Gaponik,D.V.Talapin, A.L. Rogach, K. Hoppe, E. V. Shevchenko, A. Kornowski, A. Eychmul- ler,H.Weller, J. Phys. Chem. B 2002, 106,7177. [42] DataonthePCmembranepropertiescanbefoundat:http://www.millipore. com/catalogue.nsf/docs/C153. [43] D.Wang,F.Caruso, Chem. Mater. 2002, 14,1909. ProbingofFunctionalizedMesoporousSilica NanoparticlesUsingTransitionMetalClusters** By Sophie Hermans , Sajanikumari Sadasivan, Catherine M. G. Judkins , Brian F. G. Johnson, Stephen Mann,and Deepa Khushalani* Immobilization of organometallic complexes in confined spaces has seen a great surge of interest since the advent of mesoporous materials in the 1990s. [1,2] This has been led by two main factors. Firstly, mesoporous materials are unique in thattheyofferasubstratethatcombinesthefavorableproper- ties of crystalline microporous materials (zeolites) with those ofamorphoussilica.Indeed,thesematerialspossessanintrin- sicorderedporosity(withnarrowporesizedistributions)that can be easily tuned, which results in exceedingly high surface areas (up to 1300 m 2 g ±1 have been measured). Secondly, the highlyorderedintraporousspaceofthesematerialsimposesa stabilizing environment that can be readily modified. Pore confinement implies that a stabilizing effect exists since the reactive sites are protected from deactivation and leaching effects(encapsulationphenomenon).Theimmobilizedorgan- ometallic species display structural integrity, even under sin- COMMUNICATIONS Adv. Mater. 2003, 15,No.21,November4 DOI: 10.1002/adma.200305350 Ó 2003WILEY-VCHVerlagGmbH&Co.KGaA,Weinheim 1853 ± [*] Dr. D. Khushalani SchoolofPhysicalSciences UniversityofKentatCanterbury CT27NRKent(UK) E-mail:D.Khushalani@ukc.ac.uk Dr.S.Hermans, [+] Dr.C.M.G.Judkins,Prof.B.F.G.Johnson DepartmentofChemistry,UniversityofCambridge LensfieldRoad,CB2IEWCambridge(UK) S. Sadasivan,Prof. S. Mann SchoolofChemistry,UniversityofBristol BS81TSBristol(UK) [+] Current address: UniversitØ Catholique de Louvain, UnitØ CMAT, Place LouisPasteur1bte3,B-1348Louvain-La-Neuve,Belgium. [**] We acknowledge the University of Bristol for an ORS award for SS, NewnhamCollege,Cambridge,foraResearchFellowshiptoSH,andthe EPSRCandICIforfundingforCMGJ.