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It s possible to use the DTD to designate one of the attributes as the ID specifier for a node. This ID can then be used to locate the node. It is the same idea as specifying some field in the record of a database as being the key and then using the individual key values to locate the records. An Element node can have one, and only one, of its attribute names designated as its ID. For an attribute to be used as an ID, it must be declared as such in the DTD, as shown in the example in Listing 7.29. Whenever a search is made for the ID value, the name of the attribute is not involved; it s the value of the attribute that s used to locate the Element node This means that the attribute value must be unique for the entire document, even if different elements are defined with ID attributes of different names. If there are duplicate attribute values, a search will find one of them, but there is no way to know ahead of time which one it will be. As shown in Listing 7.29, the ID named nick is defined as an attribute of the "name" element. The XML contains three "name" elements, each of which contains its

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Location coordinates can be negative when moving the mouse to a second monitor to the right or above the current monitor. The following example, FindTheMouse, illustrates the old and new methods for finding the location of the mouse on the screen.

On the left side of the equation experimental results are reduced to one number which by the expression on the right side is interpreted in terms of the order parameters and the orientation of the related transition moment On first glance it seems that S and D can be evaluated from the bands due to any two transitions of different, but well known orientations within a rigid molecule However, this is possible only with quite limited accuracy due to the anisotropy of the internal field This field originates from the dipole moments being induced in the individual molecules by the external radiation field Its anisotropy is a consequence of the molecular alignment and impedes the comparison of different bands Several approaches how to evaluate and to eliminate the influence were proposed (Neugebauer, 1954; Vuks, 1966; Haller et al.

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Decision f(1)

, 1973; de Jeu and Bordewijk, I978), however at least for the infrared range convincing results for practical applications have not been reported yet The influence could be minimized by evaluating the dichroic ratios related to two spectrally neighboured bands the transition moments of which are parallel to one of the molecular transverse axes each: Due to the uniaxiality of the phase these bands should be similarly influenced, so that reliable information on D results (Korte, 1983; Lampen, 1991) To be sure about the transition moments being strictly parallel to one of the three molecular axes, the symmetry of the molecules should be C ,, or D2h (Michl and Thulstrup, 1986), what in strict sense is hardly found with mesogenic molecules On the other hand, just the fact that a dichroism band is negative - leading to R < 1 and a negative value on the left side of Eq.

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