C08G79/02

Resveratrol-based flame retardant materials

A process of forming a resveratrol-based flame retardant small molecule with a phosphonate/phosphinate molecule that includes a chloride group and a terminal functional group.

Resveratrol-based flame retardant materials

A process of forming a resveratrol-based flame retardant small molecule with a phosphonate/phosphinate molecule that includes a chloride group and a terminal functional group.

FLAME RETARDANT POLYMERS AND METHODS OF MAKING

Polymers useful for imparting flame resistance to fibers and textiles are provided herein. The polymers are water-soluble, phosphine oxide-containing polymers that may be reaction products of hydroxymethyl phosphonium salts or hydroxymethyl phosphines with linking monomers, wherein at least 20% of the phosphorous atoms of the polymer are present as phosphine oxides. Formulations including the polymers and methods of using the polymers to impart flame resistance to fibers and textiles are also disclosed.

MODIFIED POLYMER POLYOLS

The present invention relates to new modified polymer polyols comprising at least one polyol and a stable dispersion of polymeric particles in the at least one polyol. The dispersed polymeric particles having a high content of P and N. There are also disclosed processes for the preparation of the herein described modified polymer polyols, and processes for preparing polyurethane materials containing them.

MODIFIED POLYMER POLYOLS

The present invention relates to new modified polymer polyols comprising at least one polyol and a stable dispersion of polymeric particles in the at least one polyol. The dispersed polymeric particles having a high content of P and N. There are also disclosed processes for the preparation of the herein described modified polymer polyols, and processes for preparing polyurethane materials containing them.

CELL INTERNALIZING COMPOUNDS

Provided herein are cell penetrating compounds having the Formula I:

##STR00001##

where, generally, each T is a thiol reactive group (e.g., a phosphorothioate), each L is a linker (e.g., a linear alkyl), and Y is a biologic (e.g., an antibody). Also provided are pharmaceutical compositions including the cell penetrating compounds, and methods of delivering the compound into a cell.

Cell internalizing compounds

Provided herein are cell penetrating compounds having the Formula I: ##STR00001##
where, generally, each T is a thiol reactive group (e.g., a phosphorothioate), each L is a linker (e.g., a linear alkyl), and Y is a biologic (e.g., an antibody). Also provided are pharmaceutical compositions including the cell penetrating compounds, and methods of delivering the compound into a cell.

Cross-linkable flame retardant materials

A cross-linkable flame retardant material includes a terminal furan-containing flame retardant moiety. The terminal furan-containing flame retardant moiety includes a furan moiety bonded to a phosphorus moiety via a phosphoryl linkage or via a phosphinyl linkage.

Polyphosphazene polyelectrolytes and uses thereof

Polyphosphazenes polyelectrolytes. The polyphosphazenes can be prepared by substituting pendant groups (e.g., ionic groups or pendant groups that can form ionic groups) onto a reactive macromolecular precursor for example, by reaction between the reactive chlorine atoms on the backbone of poly(dichlorophosphazene) and appropriate organic nucleophiles. In certain examples, one or more charged pendant groups of a polyphosphazene is/are further modified to introduce desired counterions, which can be hydrophobic counterions. The polyphosphazenes can activate distinct Toll-Like Receptors (TLRs) and can be used in methods of stimulating an immune response.

PROCESSES FOR PREPARING PHOSPHORODIAMIDATE MORPHOLINO OLIGOMERS VIA FAST-FLOW SYNTHESIS

Provided herein are processes for preparing an oligomer (e.g., a morpholino oligomer). The synthetic processes described herein may be advantageous to scaling up oligomer synthesis while maintaining overall yield and purity of a synthesized oligomer.