Provided is a heat-curable resin composition having an excellent workability, and capable of yielding a cured product having both a heat resistance and a low water-absorption property. The heat-curable resin composition contains: (A) a cyanate ester compound having in one molecule at least two cyanato groups, and having a cyanate ester group equivalent of 50 to 140; (B) a cyanate ester compound having in one molecule at least two cyanato groups, and having a cyanate ester group equivalent of 150 to 500; and (C) a curing accelerator,
in which the cyanate ester compound (A) is in an amount of 20 to 85% by mass per a total of 100% by mass of the components (A) and (B), and the cyanate ester compound (B) is in an amount of 15 to 80% by mass per the total of 100% by mass of the components (A) and (B).

Boron nitride nanotube (BNNT)-polyimide (PI) and poly-xylene (PX) nano-composites, in the form of thin films, powder, and mats may be useful as layers in electronic circuits, windows, membranes, and coatings. The processes described chemical vapor deposition (CVD) processes for coating the BNNTs with polymeric material, specifically PI and PX. The processes rely on surface adsorption of polymeric material onto BNNTs as to modify their surface properties or create a uniform dispersion of polymer around nanotubes. The resulting functionalized BNNTs have numerous valuable applications.

The present invention can provide a salt capable of producing a resist pattern with satisfactory CD uniformity (CDU), and a resist composition.

A resist composition comprising a resin including a structural unit having an acid-labile group, an acid generator and a compound represented by formula (I):

##STR00001##

wherein, in formula (I), R.sup.1 represents a hydrocarbon group having 1 to 36 carbon atoms which may have a substituent, X.sup.1 represents *COO, *OCO, *OCOO or *O, and * represents a bonding site to R.sup.1, L.sup.1 represents a single bond or a hydrocarbon group having 1 to 36 carbon atoms which may have a substituent, and CH.sub.2 included in the hydrocarbon group may be replaced by O, S, CO or SO.sub.2, R.sup.2 represents a saturated hydrocarbon group having 1 to 12 carbon atoms, u1 represents an integer of 0 to 2, s1 represents 1 or 2, t1 represents 0 or 1, in which s1+t1 is 1 or 2, n represents an integer of 2 or more, and a plurality of X.sup.1, L.sup.1, s1, t1, R.sup.2 and u1 each may be the same or different from each other.

The present invention addresses the problem of providing a block copolymer which is useful as a surface treatment agent for cell culture substrates, said surface treatment agent enabling cell separation in a short period of time. The above-mentioned problem is solved by a block copolymer that includes the following blocks (A), (B) and (C):(A) a temperature-responsive polymer block that has a lower critical solution temperature (LCST) within the range of from 0 C. to 50 C. with respect to water (B) a hydrophilic polymer block that does not have an LCST within the range of from 0 C. to 50 C., while having an HLB value within the range of from 9 (inclusive) to 20 (exclusive) (C) a hydrophobic polymer block that does not have an LCST within the range of from 0 C. to 50 C., while having an HLB value within the range of from 0 (inclusive) to 9 (exclusive).

A method for producing graphene, configured for forming a graphene layer on a surface of an object. The method includes steps of: depositing a poly-p-xylene material layer on the surface: and converting the poly-p-xylene material layer into a graphene layer by using a laser sintering process or a plasma-assisted sintering process.

This invention provides a resin composition for preparing an allylphenol-maleimide copolymer used for a protective film for an electronic component including: (A) an allyl group-containing phenol compound having a rigid structure; (B) an N-aromatic maleimide group-containing compound having a rigid structure; and (C) an N-aliphatic maleimide group-containing compound having a flexible structure.

The present invention relates to a composition for a gel polymer electrolyte and a gel polymer electrolyte prepared using the same, and specifically provides a composition for a gel polymer electrolyte including a lithium salt, an organic solvent, and a polymer A having an epoxy group represented by Formula 1, and a polymer B having an amine group and a cyanide group represented by Formula 2, wherein the polymers A and B are included in an amount of 1 to 20 wt % based on the total weight of the composition for a gel polymer electrolyte, and wherein a gel polymer electrolyte for a secondary battery can be prepared that includes a polymer network formed by combining the polymer A having an epoxy group represented by Formula 1 and the polymer B having an amine group and a cyanide group represented by Formula 2 in a three-dimensional structure.

The present disclosure provides cis-polycycloolefins and methods for forming cis-polycycloolefins typically having 50% or greater cis carbon-carbon double bonds comprising contacting a first cyclic hydrocarbyl monomer with a catalyst represented by Formula (I):

##STR00001##

wherein: M is a group 8 metal; Q.sup.1, Q.sup.2, and Q.sup.3 are independently oxygen or sulfur; each of R.sup.1 and R.sup.4 is a halogen; R.sup.9 is C.sub.1-C.sub.40 hydrocarbyl or C.sub.1-C.sub.40 substituted hydrocarbyl; and each of R.sup.2, R.sup.3, R.sup.5, R.sup.6, R.sup.7, R.sup.8, R.sup.10, R.sup.11, R.sup.12, R.sup.13, R.sup.14, R.sup.15, R.sup.16, R.sup.17, R.sup.18, and R.sup.19 is independently hydrogen, halogen, C.sub.1-C.sub.40 hydrocarbyl or C.sub.1-C.sub.40 substituted hydrocarbyl. In at least one embodiment, a polycyclopentene has 50% or greater cis carbon-carbon double bonds.

A light diffusing sheet according to an embodiment of the invention may be a light diffusing sheet that is formed on one side of a substrate and has a particular pattern formed on a surface thereof, where the light diffusing sheet may include a polydimethylsiloxane (PDMS) coating layer that is formed on one side of the substrate and a poly-chloro-p-xylene coating layer that is formed on one side of the polydimethylsiloxane (PDMS) coating layer with a pattern formed on its surface, the tensile strength of the polydimethylsiloxane (PDMS) coating layer is 10 to 60 psi, and a compressive force is applied on the polydimethylsiloxane (PDMS) coating layer when an interface is formed between the polydimethylsiloxane (PDMS) coating layer and the poly-chloro-p-xylene coating layer.

The present invention provides a selective bonding method of polymer substrates. The present invention allows selective interfacial bonding between a polymer substrate and a parylene layer by using a mask pattern and plasma treatment, and enables the formation of a three-dimensional structure by injecting a fluid into a non-bonded area.