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Oligomers molecular structure

Figure 3. (A) Geometry and atom labeling of PPV oligomers. Molecular structure was optimized using the Austin model 1 (AMI) semiempirical modeP in Gaussian 98 package (B) Absorption spectrum of PPV(IO). Dashed line experimental absorption of a PPV thin Solid... Figure 3. (A) Geometry and atom labeling of PPV oligomers. Molecular structure was optimized using the Austin model 1 (AMI) semiempirical modeP in Gaussian 98 package (B) Absorption spectrum of PPV(IO). Dashed line experimental absorption of a PPV thin Solid...
Linear polymers are the most commonly found, and consist of chains of D units endblocked by a variety of functionalized M units. Branched-chain silicones consist mainly of D units, with a D unit being replaced by a T or a Q unit at each point of branching. Cyclic PDMS oligomers are also common and can play a role in adhesion. They are usually found as mixtures of structures going from three siloxy units, to four, five, and higher siloxy units. A whole range of analytical techniques can determine the detailed molecular structures of these materials [20,21],... [Pg.680]

Figure 29 Some of the molecular structures used to interpret the EPR spectra of poly(aniline) oligomers. The molecules are labelled 1 and 4 in the same fashion as Ref. [149]. Figure 29 Some of the molecular structures used to interpret the EPR spectra of poly(aniline) oligomers. The molecules are labelled 1 and 4 in the same fashion as Ref. [149].
Monodisperse analogs of such ir-electron systems, PPV oligomers (molecular glasses) were studied by Bazan and coworkers [217]. The films prepared from 192 by solution casting showed completely amorphous structure due to a tetrahedral structure of the molecule and OLEDs ITO/PVK/192/Al-emitted green light with an efficiency up to 0.22 cd/A (Chart 2.42). [Pg.97]

Some of the molecular structures of alkoxy alanes or siloxy alanes have been obtained from single-crystal X-ray structure determination. In order to demonstrate the diversity of agglomeration of the monomeric species to oligomers or polymers, we will discuss some typical structures. [Pg.84]

II Conjugation alone cannot be relied upon to significantly enhance the optical nonlinearities. The conformational effects and the role of the substituents so that understanding of the molecular structure-property relation can be improved have been studied (89JPC7916). In the case of the thiophene oligomers, a rapid increase in the y value (large microscopic nonlinearity) as a function of N is found. [Pg.293]

It is exceedingly difficult to determine the molecular structure of a synthetic macromolecule. X-ray diffraction—the ultimate structural tool for small-molecule studies—yields only limited information for most synthetic high polymers, and crucial data about bond lengths and bond angles are difficult to obtain.47 However, that same information can be obtained relatively easily from single crystal X-ray diffraction studies of cyclic trimers, tetramers, and short-chain linear phosphazene oligomers. The information obtained may then be used to help solve the structures of the high polymeric counterparts. [Pg.100]

As the X-ray diffraction diagrams of an oriented gel (Fig. 6) are poorly crystalline, it has been useful to conduct X-ray crystal structure analyses of oligomer of 3-(l->-3)-D-glucan. The molecular structures of laminarabiose and its acetyl derivative have been determined. [Pg.367]

Oligoorganosiloxanes are widely used in various fields of industiy. As a rule, they are transparent, colourless, stable liquids with a rather low molecular weight (from 160 to 25 000) according to their molecular structure they are divided into cyclic and linear oligomers. Because of their valuable characteristics, oligoorganosiloxanes are often more practical than organic liquids. [Pg.462]

T. Malfait, H. Van Dael, and F. van Cauwelaert, Molecular structure of carrageenans and kappa oligomers A Raman spectroscopic study, Int. J. Biol. Macromol., 11 (1989) 259—264. [Pg.196]

Depending on the substitution pattern of the monomers, different kinds of cross-linking can be anticipated, which can lead to small oligomers, but also to rings, chains, or polydimensional networks [1]. This applies to standard benzene derivatives, as well as to condensed arenes with more sophisticated molecular structures. These products are interesting in their own right owing to their physical and opto-physical properties, but also as precursors for refractory materials prepared in pyrolysis or plasma processes [1]. [Pg.4]

Figure 7 Molecular structures and schematic representations of a bis-CA and a tris-M that do not self-assemble to form the proposed tetrahedral aggregate oligomers are formed preferentially... Figure 7 Molecular structures and schematic representations of a bis-CA and a tris-M that do not self-assemble to form the proposed tetrahedral aggregate oligomers are formed preferentially...
In general, borates are structurally complex, since the boron atoms can be in 3 and/or 4 coordination and oligomer, ring, and chain polymers are all found (Christ and Clark, 1977 Wells, 1975). We shall not attempt to describe fully the complexity of these structures but will concentrate on the fundamental polyhedral units. The molecular geometric and electronic structures of these materials can be studied using many of the site-specific spectroscopies previously discussed. The bulk properties of the materials also change, of course, depending upon the molecular structure. [Pg.260]

Fig. 3. NMR spectra of p-PDA Et, its oligomer, dimer and polymer, and peak assignment to their molecular structures. Figures in parentheses indicate the reaction temperature, (source Ref. 29)... Fig. 3. NMR spectra of p-PDA Et, its oligomer, dimer and polymer, and peak assignment to their molecular structures. Figures in parentheses indicate the reaction temperature, (source Ref. 29)...
Thus, the presented results show that the type of viscosity variation at gelation is determined, first, by a variation of molecular structure of the oligomer and, second, by a phase separation in the system near the point of relaxation transition, i.e., gelation. [Pg.237]

It should be noted however that though the smaller size of CO2 molecules (as compared to hexene molecules) may impart better transport properties to the SCF reaction mixture, oligomer extraction may actually be hindered by the presence of CO2 due to (a) lower reaction temperature and hence lower vapor pressure for the oligomers, and (b) greater disparity between molecular structures of COo and the oligomers. [Pg.312]

The name calixarene derives from the Greek word for a vase, which aptly describes their molecular structure. The structures of the para-t-butyl calix[n]arenes (n = 5, 6, 7, 8) (1)—(4) differ only in the size of the ring oligomer. Other ring sizes are available, but few metal ion complexes have been isolated with them. [Pg.485]


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