With fiber optical telecommunication systems penetrating into metropolitan and access networks, planar waveguide technology is increasingly being considered a solution to the bottleneck of cost-effective manufacture of passive components. Being recognized for their high thermo-optical coefficients, ease of fabrication, cost-effectiveness, and compatibility with other materials, polymers as a platform technology for waveguide devices are gaining more and more commercial acceptance. Fully exploiting the potentials of the polymeric materials demands comprehensive understanding of both the specific device applications and various polymer systems. The right choice of materials is often the key to the success of component development. Unfortunately, since extensive study of polymeric materials and devices operating at 1.55 m began just recently, few ideal materials have so far been made commercially available. From the polymer chemistry point of view, it is possible to tailor the materials to meet specific and strict requirements for optical waveguide devices. This is a review of the most promising fluorinated polymers and silicone resins and their demonstrated device applications. The paper is designed to provide a guide to both polymer scientists who want to develop novel high-performance materials for waveguide applications, and optical engineers who need to gain insight into the materials.
Highly fluorinated poly(ether sulfone)s were prepared by a modified polycondensation technique, using a molecular sieve dehydrating apparatus in order to efficiently remove water under mild conditions. Consequently, side reactions were minimized, which resulted in the formation of polymers free of microgels. This reaction was also used to introduce pentafluorostyrene moieties into the polymer to provide crosslinking functionalities.
An efficient and highly enantioselective catalytic asymmetric hydrogenation of β-acylamino nitroolefins has been realized by using Rh-TangPhos as the catalyst. A series of β-amino nitroalkane products, which are versatile intermediates in organic synthesis, were obtained with high yield and good enantioselectivity.
The asymmetric hydrogenation of β-amino nitroolefins has been successfully achieved by rhodium/bis(phosphine)-thiourea L1 with excellent enantioselectivities and yields (up to 96% ee, 96% yield, >99% conversion, TON up to 1000) under mild conditions. Chiral β-amino nitroalkane products and their derivatives are versatile intermediates in organic synthesis.
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