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.NET Remoting Technology Projection connected to the server. The on-the-fly code generation is made possible by the Reflection.Emit namespace s classes, which can be used to generate MSIL code at runtime, packaging it into an in-memory assembly for direct execution in the running CLR instance. To find out about the interface of the remote object (the interface that must also be used for the generated transparent proxy), the client runtime uses reflection on the type parameter given in the Activator.getObject call. So what exactly is the interface of a remote object .NET does not require developers to define an explicit interface for remote objects. By default, the public methods of the remote object class constitute the interface of the remote object. To allow the client to use reflection to build the transparent proxy, this implies that the implementation of the remote object is actually available to the client. However, it is not good design practice to transfer the implementation class s code to the client merely to invoke remote operation invocations. It is therefore good practice to define an explicit interface for remote objects, as illustrated in the following code fragments.

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The Curses library of terminal control functions has been with UNIX since the early 1980s. As such, it was part of the older versions of UNIX, which required complex licenses and such to be used. NCurses is the New Curses software emulation of the original Curses and is available from the GNU folks at the Free Software Foundation. Odds are pretty good that the computer system you re using employs NCurses, not the original Curses. Because of that, this book uses NCurses to refer to the library and its functions. The book is current with NCurses version 5.5.

Azo chiral:

In this book, you ll find the following conventions used:

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C language keywords, function names, or prompt commands are listed in monospace type, such as: if or newwin() or ls -l. Filenames are listed in monospaced caps, such as A.OUT or GOODBYE.C. Directory and pathnames are also in small caps: ~/PROG/C/CURSES Program code appears with the source code filename first, followed by the code:

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the cis-azobenzene. Thus, the shape of the azobenzene molecule in uences the molecular orientation of a host LC (Sanpei, 2005).

1 2 3 4 5 6 7 8 9 10 11 12 13 #include <ncurses.h> int main(void) { initscr(); box(stdscr, * , * ); refresh(); getch(); endwin(); return 0; }

The line numbers, to the left of the bar, are for reference only; do not type them. The code is to the right of the bar.

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In binary Ch LC systems consisting of the chiral compound and the host nematic LC, the intermolecular interaction between the chiral azobenzene molecule and LC molecule contributes to HTP of the chiral azobenzene compounds. In this section, photoswitching behavior of some chiral azobenzene compounds (Fig. 10.7) is examined in terms of the in uence of the chiral groups on the photochemical change in HTP. Figure 10.10 shows changes in absorption spectra of p-azo-7 in methanol and in E44 by UV irradiation. The absorption spectra are characterized by a strong absorption at 370 nm corresponding to p p* transition of trans form and a weak absorption at 450 nm, which originates from the n p* transition of cis form. Upon UV irradiation, absorbance at B370 nm was decreased because of the trans cis photoisomerization with an increase in low intensity band at around 450 nm.

The remote object hosted by the server then has to implement this interface:

The programs in this book are short and to the point. As such, they rarely include comments. Even so, be sure to comment your own code and name your variables in a friendly way. Some programs later in the book dispense with error-checking for some NCurses procedures. This is noted as a bad practice in real life but is done here to keep the code short and easy to read and type. In your code, always be sure to check for errors with those NCurses functions that can return errors, as noted in the text.

Change in the orientation order S by replacing with different chiral dopant. Host/Dopant 5CB 5CB /trans-p-Azo-9 5CB /cis-p-Azo-9 Ratio, mol/mol 50/0 49/1 49/1 S Before 0.53 0.53 0.53 After 0.51 0.66 0.54 S, % 3.8 +19.7 +1.9

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