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Capsule orientation

The option of the use of a capsule sorting apparatus this is an empty capsule orienter to drive the capsules in the right position. [Pg.643]

Input from A. E. Newton, especially concerning capsule orientation terminology, and from an unknown reviewer significantly improved this paper. [Pg.240]

There are two main types of plug forming machines the dosator type (e.g., MG2, Zanasi, and Matic machines) and the dosing disc type (e.g., Bosch GKF, Impressa, and Index machines). Bosch GKF machines were formerly manufactured by Hofliger and Karg (H K). Both types of machines have capsule rectification and separation operations in common. As empty capsules are fed into these machines, they are first rectified, i.e., oriented so that they are delivered body-end down into split bushings. [Pg.410]

However, great care must be taken in choosing an appropriate sample holder and a suitable sample geometry.9 Cylindrical capsules machined from high-purity PTFE, enclosed in long polyethylene straws, allow the measurement of compressed polycrystalline samples or even solutions. Polycrystalline samples need to be pulverized so that preferential orientation can be avoided. The sample should be placed into a cylindrically shaped sample holder. Air-sensitive compounds can be sealed in small tubes from synthetic quartz glass. The field- and temperature-dependent contribution of the sample holder must be known precisely. [Pg.83]

Opium is obtained from the dried juice from the seed capsule of the oriental poppy, Papaver somniferum. The dried juice contains up to 17% morphine and 4% codeine by weight, as well as other, non-additive alkaloids that lack analgesic activity such as noscapine, papaverine, and thebaine. Papaveretum is a standardized preparation of opium containing 50% morphine. [Pg.389]

Definitive location of all guest molecules inside the cavity is somewhat ambiguous owing to inexact stoichiometry and disorder. However, the (+)-MALDI mass spectra of II indicate that each individual capsule encloses different mixtures of water and acetone. In particular, two peaks implicated the presence of 24 entrapped water molecules that occupy axial coordination sites orientated toward the center of the cavity. [Pg.799]

Coencapsulation is a process that limits the space provided to trapped guests and obliges them to sense reciprocally simply because they cannot avoid each other. Chirality is a feature related to the spatial distribution of objects, therefore any symmetric closed space becomes chiral if a chiral object is placed in it (Fig. 27A). This simple concept is then applied to spherical and cylindrical capsules in both cases the correct orientation of two chiral guests is necessary to allow interactions between the asymmetric centers of the two partners. In... [Pg.38]

Fig. 27 A A chiral object like a hand in an achiral environment leaves a chiral space available. B Spherical supramolecular capsules are much less suitable compared to C cylindrical ones for enantiorecognition because of the greater number of possible reciprocal orientations of two co-guests encapsulated... Fig. 27 A A chiral object like a hand in an achiral environment leaves a chiral space available. B Spherical supramolecular capsules are much less suitable compared to C cylindrical ones for enantiorecognition because of the greater number of possible reciprocal orientations of two co-guests encapsulated...
Fig. 19 Formation of the dimeric coordination capsule 28 based on the calixarene ligand 27. The helical twist results from the orientation of the meta-substituted pyridyl units upon coordination to palladium(II) ions (represented by grey spheres). Adapted with permission from [141]. Copyright 2001 American Chemical Society... Fig. 19 Formation of the dimeric coordination capsule 28 based on the calixarene ligand 27. The helical twist results from the orientation of the meta-substituted pyridyl units upon coordination to palladium(II) ions (represented by grey spheres). Adapted with permission from [141]. Copyright 2001 American Chemical Society...
Scheme 3.10 Closed spaces inside a capsule impose restrictions in the orientation of reaction partners in a 1,3-dipolar... Scheme 3.10 Closed spaces inside a capsule impose restrictions in the orientation of reaction partners in a 1,3-dipolar...
Scheme 3.11 Chirality in a heterodimeric ureidocalix[4]arene capsule, induced by the orientation of the cyclic array of hydrogen bonds. Scheme 3.11 Chirality in a heterodimeric ureidocalix[4]arene capsule, induced by the orientation of the cyclic array of hydrogen bonds.
The relatively low thermodynamic stability of complexes of hemicarcerands or other container-type hosts is a direct consequence of structural aspects of the walls that make up the inner surface of such compounds. These walls are lined by aromatic subunits while free electron pairs of heteroatoms such as those of the ether oxygen atoms are preferentially oriented to the outside. Complexes are therefore enthalpically stabilized only by weak dispersive interactions. In the case of positively charged guests cation-re interactions can contribute to binding enthalpy as in a self-assembled calixarene-derived capsule [9], but directed interactions such as hydrogen-bonding interactions are usually absent. [Pg.5]

There are many kinds of capsules but few have the capacity to position co-guests in predictable orientations. We used the ability of 1.24.1 to do so, and applied it to evaluate hydrogen-bonding interactions between boronic acids, carboxylic acids, and primary amides [52], The phenyl boronic acids are useful as components of covalently self-assembled systems [53], and we found that the p-methyl, methoxy, ethyl, and isopropyl derivatives all fit as symmetrical dimers inside I.24.I. The structure of the boronic acid dimer has been debated but a recent theoretical study found the doubly hydrogen-bonded exo/endo conformer (Fig. 10) to be lowest in... [Pg.65]

Kobayashi K, Ishii K, Sakamoto S, Shirasaka T, Yamaguchi K (2003) Guest-induced assembly of tetracarboxyl-cavitand and tetra(3-pyridyl)-cavitand into a heterodimeric capsule via hydrogen bonds and CH-halogen and/or CH-n interaction control of the orientation of the encapsulated guest. J Am Chem Soc 125 10615... [Pg.123]


See other pages where Capsule orientation is mentioned: [Pg.409]    [Pg.11]    [Pg.204]    [Pg.240]    [Pg.240]    [Pg.241]    [Pg.409]    [Pg.11]    [Pg.204]    [Pg.240]    [Pg.240]    [Pg.241]    [Pg.21]    [Pg.213]    [Pg.347]    [Pg.199]    [Pg.207]    [Pg.158]    [Pg.12]    [Pg.14]    [Pg.434]    [Pg.248]    [Pg.410]    [Pg.679]    [Pg.900]    [Pg.30]    [Pg.31]    [Pg.798]    [Pg.16]    [Pg.39]    [Pg.40]    [Pg.41]    [Pg.103]    [Pg.98]    [Pg.97]    [Pg.191]    [Pg.23]    [Pg.24]    [Pg.31]    [Pg.31]    [Pg.109]    [Pg.120]   
See also in sourсe #XX -- [ Pg.5 , Pg.11 , Pg.204 ]




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