Green excitable tandem dyes are provided. Tandem dyes of embodiments of the invention include: a non-conjugated polymeric backbone; one or more green excitable donor fluorophores linked to the non-conjugated polymeric backbone; and one or more acceptor fluorophores linked to the non-conjugated polymeric backbone; where the donor and acceptor fluorophores are in energy transfer relationship. Also provided are methods of making and using the tandem dyes, as well as kits that include the dyes and find use in embodiments of the methods.

A high-sensitivity, high-selectivity and portable detection method for trace uranyl ion is described. The method has an ultralow detection limit of 11 pM/2.6 ppt and is useful in precise monitoring of the uranium content in agricultural and sideline products, foods, environments and so on. The test instrument is miniaturized and low in cost to achieve high-precision portable measurement in the field. A conjugated polymer with aggregation-induced emission (AIE) activity is synthesized, and prepared into Pdots, and a uranyl-responsive electrochemiluminescence (ECL) probe is developed by modifying the Pdots with DNA or RNA, which serves as an adsorption ligand of uranyl ion. The probe exhibits good biocompatibility. The ECL technology can be used in uranyl ion detection and the method has extremely high sensitivity. A uranyl ion probe with AIE activity is also disclosed, which can be applied in portable precise monitoring of trace uranyl ion by means of the ECL technology.

An all-donor black color electrochromic polymer is disclosed as well as a method for preparing the all-donor black color electrochromic polymer. The electrochromic polymer comprises conjugated polymers, and the conjugated polymers are chemically linked, or physically blended, or both.

Electrochromic polymers include conjugated chromophores in spaced relation with one another, and conjugation-break spacers (CBSs). At least one CBS separates adjacent chromophores. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidization states.

Various photocrosslinkable electrochromic polymers are disclosed. The polymers are suitable for an electrochromic layer of an electrochromic device. The polymers are formed with a two-step synthesis method that includes forming a polymer precursor with one or more chromophore blocks, and mixing the polymer precursor with photocrosslinkable monomer units to form the polymer.

A redox reversible fluorescent probe for performing single-electron transfer fluorescence probing includes: a redox moiety including: a terminal moiety; an electron transfer metal coordinatively bonded to the terminal moiety; and a bridge moiety coordinatively bonded to the electron transfer metal; and a fluorescent moiety covalently bonded to the bridge moiety of the redox moiety and comprising: an electron bandgap mediator that is covalently bonded to the bridge moiety; a coordinate center covalently bonded to the electron bandgap mediator and that forms a Zwitterionic member with an atom in the electron bandgap mediator; and a steric hinder bonded to the electron bandgap mediator to provide steric hindrance for protection of the coordinate center.

The present invention relates to compounds of the formula (1) and (2) which are suitable for use in electro¬nic devices, in particular organic electroluminescent devices.

The invention relates to a security pigment, comprising core-shell particles having a core based on an organic addition polymer, a shell based on an organic condensation polymer and a feature substance present in the core in finely dispersed or dissolved form, wherein the addition polymer is a three-dimensionally cross-linked duromer.

This disclosure relates generally to electrochromic polymers that include a plurality of -conjugated chromophores in spaced relation with one another, and a plurality of conjugation-break spacers (CBSs), where at least one CBS separates adjacent chromophores. The chromophores may be colored in the neutral state, and multicolored to transmissive in different oxidization states.

Various photocrosslinkable electrochromic polymers are disclosed. The polymers are suitable for an electrochromic layer of an electrochromic device. The polymers are formed with a two-step synthesis method that includes forming a polymer precursor with one or more chromophore blocks, and mixing the polymer precursor with photocrosslinkable monomer units to form the polymer.