N-Hexyl isocyanate

C22H40O3 111466-59-2) see Orlistat (35,45)-3-hexyl-4 [(27f)-2-hydroxytridecyl]-2-oxetanone (C22H42O3 104872-06-2) see Orlistat n-hexyl isocyanate... 

A few synthetic helical polymers are known to act as chiral selectors.7a,918d l8k i9d i9h ancj are widely used as chiral stationary phases (CSP) in gas or liquid chromatography.73,53 Recently, it has been reported that the preference of one helical sense in isotropic solution can be induced by some interaction between optically inactive polymers and chiral solvents/additives. Examples of this include poly(n-hexyl isocyanate)18d l8k and poly(phenylacetylene)s bearing functional group.19d 19h The polysilane derivatives also show chiral recognition ability in solution at room temperature. Poly(methyl-ft-pinanylsilane) includes two chiral centers per bulky hydrophobic pinanyl side group28 and... 

Itou et al. [60] determined 0II/0C for isotropic solutions of poly(n-hexyl isocyanate) (PHIC) and dichloromethane (DCM) from sedimentation equilibrium data on narrow distribution PHIC samples. Figure 3 shows their results, where the ordinate Mw(0II/0c) represents the osmotic pressure increment on the molar concentration scale. 

Fig. 7. Comparison of experimental phase boundary concentrations between the isotropic and biphasic regions for various liquid-crystalline polymer solutions with the scaled particle theory for wormlike hard spherocylinders. ( ) schizophyllan water [65] (A) poly y-benzyl L-glutamate) (PBLG)-dimethylformamide (DMF) [66-69] (A) PBLG-m-cresoI [70] ( ) PBLG-dioxane [71] (O) PBLG-methylene chloride [71] (o) po y(n-hexyl isocyanate) (PHICH°Iuene at 10,25,30,40 °C [64] (O) PHIC-dichloromethane (DCM) at 20 °C [64] (5) a po y(yne)-platinum polymer (PYPt)-tuchIoroethane (TCE) [33] ( ) (hydroxypropyl)-cellulose (HPC)-water [34] ( ) HPC-dimethylacetamide (DMAc) [34] (N) (acetoxypropyl) cellulose (APC)-dibutylphthalate (DBP) [35] ( ) cellulose triacetate (CTA)-trifluoroacetic acid [72]...

A more remarkable and dramatic change in the conformation of helical polymers upon photoirradiation has been observed for the azobenzene-modified poly isocyanates. Polyisocyanates are typical dynamic helical polymers [59,60]. Even the optically inactive poly(n-hexyl isocyanate) (20), which is devoid of stereogenic centers, exists as an equal mixture of right- and left-handed helical conformations. Equilibrium exists in solution between both helices separated by... 

Few other sets of viscosities exist for polymeric nematics. Yang and Shine (1993) obtained three of the Leslie viscosities for monodomains of poly(n-hexyl isocyanate) (PHIC) from rheological measurements in the presence of an electric field, and they obtained values reasonably consistent with the predictions of the Kuzuu-Doi expressions. From monodomains of the polyion PBZT, poly(l,4-phenylene-2,6-benzobisthiazole) in methane sulfonic acid, some of the Leslie-Ericksen parameters have been extracted via light-scattering and magnetic-field-reorientation studies (Berry 198S Srinivasarao and... 

The sensitivity of the helical preference of polyisocyanates to small chiral influences is also observed in chiral solvents. Poly(n-hexyl isocyanate) was found experimentally to have a persistence length of 20— 40 nm depending on the solvent in which the measurements were carried out.66 It was hypothesized that in more polar solvents a local interaction of the solvent would give rise to larger torsional oscillations around the backbone bonds. It was indeed observed that dissolution of poly(n-hexyl isocyanate) in non-racemic chiral solvents, e.g., (5)-l-chloro-2-methyl-butane, changed the persistence length and in addition also resulted in an excess of one helical sense.67 The chiral bias favoring one helical sense by itself is miniscule, but due to the cooperativity, a chiral preference is observed. More recently it was noted that the circular dichroism of these polymers decreases upon the addition of an achiral or racemic... 

Polymerizations with CpTiCliX were found to tolerate a wide variety of Lewis bases. The process of polymerization of n-hexyl isocyanate is... 

Figure 2. Structure of liquid crystalline block copolymers (LC-BCPs) (A) rod-coil diblock copolymer (B) rod-coil diblock copolymer with flexible spacer in the rod block (C) side group liquid crystal-coil (SGLC- coil) diblock copolymers (D) coil -rod-coil ABC triblock copolymers (predicted to be novel ferroelectric fluid by R. G. Petschek and K. M. Wiefling, Phys. Rev. Lett., 1987, 59(3), 343-346) (E) rod-rod diblock copolymer (one example of well-defined po-ly(n-hexyl isocyanate-fc-n-butyl isocyanate) rod-rod diblock copolymer was given by Novak et al. [68], however, no morphology studies were reported) (F) dendritic liquid crystal-coil (DLC-coil) diblock copolymer (not reported).

Scheme 1. Microphase separation process for LC-BCPs. Solvents have the same effect as raising temperature due to a reduced x=Xiii- Path 1 and 2 for SGLC-coil systems (e.g. SICN5 systems, see Scheme 9 for structures) path 3 for rod-coil systems (e.g. po-ly(styrene-h-n-hexyl isocyanate)).

Scheme 6. Synthesis of poly(styrene-n-hexyl isocyanate) rod-coil diblock copolymers [40, 62].

SH-Vy S stands for styrene block, H for poly(n-hexyl isocyanate) block, x for the real molecular weight of styrene block, and y for the polyisocyanate block in kg/mol. 

Ohshima, A., Kudo, H., Sato, T, and Teramoto, A., Entanglement effects in semiflexible polymer solutions 1. Zero-shear viscosity of poly(n-hexyl isocyanate) solutions. Macromolecules, 28, 6095-6099 (1995). 

OTHER POLYMERS SHOWING THIS SPEOAL PROPERTY Rigid-rod molecule, helical conformation poly(n-hexyl isocyanate), poly(7-benzyl-L-glutamate). 

OTHER POLYMERS SHOWING THIS SPEriAL PROPERTY Poly(n-hexyl isocyanate) rigid polymer backbone with bulky side chain. Triarylmethyl methacrylates high value of optical activity with helix polymer structure. 

---