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We report the observation of 3D linear or branched chains of polymer-blend microspheres generated from liquid droplets of solution where the modified surface structure of the polymer composite results in highly robust interparticle bonds. Using a linear quadrupole to precisely position particles in space, we are able to take advantage of this novel material property to actively assemble particles in programmable three-dimensional architectures. The robust interlocking nature of interparticle linkage gives rise to strongly coupled morphology-dependent resonances in bisphere and trisphere systems, suggesting the possibility of three-dimensional photonic "molecules" and microscale optical manipulation applications.

Mossbauer spectra for l and d enantiomers of the Fe(phen)3Sb2(C4H2O6)(2);8H(2)O complex are reported. Four independent experiments show a small but reproducible energy shift of the Fe-Mossbauer spectra for the two enantiomers of 0.004+/-0. 002 mm/sec ( 1.9x10(-10) eV). This exceedingly small energy difference is comparable to that predicted by the parity-violating energy difference (PVED) using a Z6.2 scaling law applied to low Z ( Z = 6) molecules. Theoretical calculations suggest that the PVED for the Fe(phen)2+3 moiety should be smaller than this estimate, however, PVED effects of the chiral antimony tartrates are not taken into account.