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For servant activators, the RETAIN policy has to be used, so that the active object map of the POA keeps track of activated servants. The servant activator can now be registered with the newly-created POA, as follows:

12 13 14 15 16 17 18



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These results unambiguously locate the photosensitive azobenzene ligands, along with surfactant, within the uniform nanopores of the self-assembled lms and emphasize the need to accommodate the steric demands of the photoisomerization process by engineering the pore size (as noted previously for adsorbed azobenzene dyes (Ogawa et al, 2000)) and positioning the photoactive species on the pore surfaces Correspondingly, nanocomposite lms prepared using the triblock copolymer surfactant P123, which had larger pores (ca 65 nm in diameter), exhibited a faster and more complete trans-cis isomerization, close to that of TSUA in EtOH solution, presumably because the azobenzene ligands were less sterically constrained It is noteworthy that there exists a difference between the UV/visible spectra of Brij 56 templated nanocomposite lms before (Fig 1312a) and after (Fig 1312b) the surfactant removal.

addstr( Red text on a cyan background.\n ); refresh(); getch(); endwin(); return 0; }

Sample output:





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MyActivator activator; PortableServer::ServantManager_var servant_manager = &activator; servant_manager_poa->set_servant_manager (servant_manager);

For the azobenzene contained in the nanocomposite lm before the surfactant removal, the p p* transition of the trans isomer is at 333 nm and the n p* transition of the cis isomer is at 440 nm After the surfactant removal, the p p* transition of the trans isomer and the n p* transition of the cis isomer are shifted to 350 and 460 nm, respectively In both situations, the absorbance of the n p* transition is quite high, indicating that the molar absorption coef cient (e) of the n p* transition is larger than that in solution owing to the out-of-plane position of the azobenzene phenyl rings This effect may be the result of steric constraint and hydrogen-bonding interactions between the azo- and silanol groups on the silica wall.

The default colors have been set to Red text on a cyan background. The text above appears as red on a cyan background.

COLORS, init_pair(), use_default_colors()

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In comparison to the azobenzene contained in the nanocomposite lm after the surfactant removal, the appearance of the p p* and the n p* transitions at lower wavelength (blueshift) before the surfactant removal indicates that the azobenzene ligands are out of plane to a larger extent The absorbance at the n p* transition of azobenzene ligands contained in P123-templated lm is lower than that in the Brij 56 templated lm, indicating a less sterically constrained environment because of the larger pore sizes of P123-templated lm The preceding UV/visible data were measured using a re ection mode For TSUA-modi ed nanocomposite thin lms coated on indium tin oxide (ITO)/glass substrates, a transmission mode was adopted to measure the absorbance of the lms In the experiment, the lm was soaked in a Tris buffer solution containing.

At this point, an object reference to the as-yet inactive remote object is created with a user-defined OBJECT ID, which allows us to identify requests for a specific servant.

attr_get()

The attr_get() function is used to read which text attributes are being used in a window. The values returned are compared (by logical OR) with known attributes. The function also determines whether the window uses color and if so which color pair is being used.

Adding substituents to the azobenzene rings may lead to minor or major changes in spectroscopic character Of particular interest is ortho- or parasubstitution with an electron-donating group (usually an amino, NH2), which results in a new class of compounds In these aminoazobenzenes, the n-p* and p-p* bands are much closer In fact, the n-p* may be completely buried beneath the intense p-p* Although azobenzenes are fairly insensitive to solvent polarity, aminoazobenzene absorption bands shift to higher energy in nonpolar solvents and shift to lower energy in polar solvents Substituting azobenzene at the 4 and 4u positions with an electron-donor and an electron-acceptor (such as an amino and a nitro, NO2, group) leads to a strongly asymmetric electron distribution (often referred to as a push pull substitution pattern) This shifts the p-p* absorption to lower energy, toward the red and past the n-p*.

int attr_get(attr_t *attrs, short *pair, void *opts); int wattr_get(WINDOW *win, attr_t *attrs, short *pair,void *opts);

PortableServer::ObjectId_var object_id = PortableServer::string_to_ObjectId ("Foo"); CORBA::Object_var object = servant_manager_poa->create_reference_with_id (object_id, "IDL:Foo:1.0");

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