摘要:
The present document provides a method and wireless device for implementing route transmission based on a single IPv6 address prefix. The method includes: when a wireless device succeeds in IPv6-based dialing and obtains one 64-bit-long IPv6 address prefix from a network side, the wireless device first setting apart a 126-bit IPv6 address prefix from the prefix, and then allocating the 126-bit IPv6 address prefix to a WAN interface, allocating the 64-bit-long IPv6 address prefix to a LAN interface, and notifying a user terminal connected to the LAN interface of the IPv6 prefix of the LAN interface, so that the user terminal connected to the LAN interface generates its own IPv6 address through a stateless address auto-configuration mechanism for communication. With the technical solutions of the present document, in an IPv4/IPv6 dual stack mode, IPv4 and IPv6 protocol stacks operate normally, and the radio resource consumption is reduced.
摘要:
A disclosed dual antenna system includes a receiving antenna which includes a first surface orthogonal to an incident wave, the first surface being a first antenna aperture, and a transmitting antenna which includes a second surface parallel to a reflection direction which is a transmission direction, the second surface being a second antenna aperture. A portion of a structure of the transmitting antenna is shared by the receiving antenna.
摘要:
A formulation including: an organic semiconducting material; and a carrier liquid including at least one of: a first liquid of the formulas (III) or (II): or mixtures of formulas (III) and (II); and a second liquid of a saturated or unsaturated cyclic hydrocarbylene compound of the formula (I): where the respective R1-8, x, and n are as defined herein, and optionally a tertiary liquid carrier, as defined herein. Also disclosed are semiconducting articles prepared with the formulations as defined herein.
摘要:
Articles utilizing strengthened glass substrates, for example, ion-exchanged glass substrates, in combination with organic molecules or polymers are described along with methods for making the articles. The articles are useful in electronics-based devices that utilize organic thin film transistors.
摘要:
Compounds that modulate the CCR5 chemokine receptor, pharmaceutical compositions containing them, and uses therefor in the treatment of HIV and related diseases are described.
摘要:
The present invention relates to tetrahydroprotoberberines of the formula (I) and the physiologically acceptable salts thereof. The invention also relates to the use of the compounds of the formula (I) or pharmaceutically acceptable salts thereof for preparing a pharmaceutical composition for the treatment of a medical disorder susceptible to treatment with dopamine receptor ligand, such as schizophrenia.
摘要:
Articles are described utilizing laminated glass substrates, for example, ion-exchanged glass substrates, with flexible glass or polymers and with semiconductor devices which may be sensitive to alkali migration are described along with methods for making the articles.
摘要:
The present invention relates to tetrahydroprotoberberines of the formula (I) and the physiologically acceptable salts thereof. The invention also relates to the use of the compounds of the formula (I) or pharmaceutically acceptable salts thereof for preparing a pharmaceutical composition for the treatment of a medical disorder susceptible to treatment with dopamine receptor ligand, such as schizophrenia.
摘要:
The present invention relates to new salts of pyrazolopyrimidinone represented by formula (I), and pharmaceutically acceptable polymorph, solvate, hydrate, dehydrate, co-crystallization, anhydrous, or amorphous form thereof, the pharmaceutical compositions, and a pharmaceutical unit dosage form containing the same, wherein x represents organic or inorganic acids, preferable maleic acid, succinic acid, methanesulfonic acid, hydrochloric acid, etc. The invention further relates to co-crystals or complexes of compounds of pyrazolopyrimidinone and pharmaceutical compositions containing the same. The present invention also relates to a process for the preparation, use thereof and pharmaceutical preparation containing the salts or crystalline forms.