2015
DOI: 10.1016/j.molstruc.2015.07.026
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Preparation, physicochemical analysis and molecular modeling investigation of 2,2′-Bipyridine: β-Cyclodextrin inclusion complex in solution and solid state

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Cited by 21 publications
(6 citation statements)
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References 64 publications
(38 reference statements)
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“…Thus, all vibrations and bends of the βCD were shifted to lower frequencies after complexation with phenanthrene. This observation is different from the reported data [ 45 , 48 ] where all vibrations and bends of the βCD were shifted to slightly higher frequencies due to the of the “guest” molecules into the βCD cavity. This difference is due to the difference in the chemical structure of the “guest” molecules, i.e., guest molecules cause the in the vibrations and bend frequencies, but the nature of the shift (blue- or redshift) would depend upon the chemical nature of the guest molecules.…”
Section: Resultscontrasting
confidence: 99%
“…Thus, all vibrations and bends of the βCD were shifted to lower frequencies after complexation with phenanthrene. This observation is different from the reported data [ 45 , 48 ] where all vibrations and bends of the βCD were shifted to slightly higher frequencies due to the of the “guest” molecules into the βCD cavity. This difference is due to the difference in the chemical structure of the “guest” molecules, i.e., guest molecules cause the in the vibrations and bend frequencies, but the nature of the shift (blue- or redshift) would depend upon the chemical nature of the guest molecules.…”
Section: Resultscontrasting
confidence: 99%
“…The fact that the morphologies of the particles are quite similar to those obtained by PM and those obtained by both KND and SL does not mean that no interaction occurred between CMO and the CDs and therefore, additional studies need to be performed in order to confirm the formation of inclusion complexes. However, modifications in the shape and aspect of surface morphology have been suggested as an indication of inclusion complex formation with CDs [ 34 , 35 ].…”
Section: Resultsmentioning
confidence: 99%
“…SEM is widely used to morphologically identify the formation of inclusion complexes due to the fact that such complexation usually involves changes in the surface, particle size and appearance of the parent drug [41]. When a drug is complexed within the CD cavity, the morphology of the obtained IC tends to be distinct from that of each individual component [42,43]. As shown in Figure 2, the morphological aspects of both ABAM- βCD and ABAM- HPβCD were markedly different from those of ABAM, βCD and HPβCD.…”
Section: Discussionmentioning
confidence: 99%