π-conjugated oligomers 1a b and 2a b, containing furan-fused and thiophene-fused aromatic units, were systematically designed and successfully synthesized.
A new series of 1,4-dihydropyridine derivatives (2a h, 3a e, and 4a e) were systematically designed and synthesized via ultrasound irradiation methods with easy work-up and good yields.
Stereological bias experiments require that the condition of the particles' internal structure can be systematically designed and the three-dimensional (3D) and 2D liberation states can be obtained.
Sensor systems that are intended to ensure the safety and well-being of building occupants should be systematically designed and their performance evaluated.
In order to achieve strict dissipativity (i.e., unity maximum transient growth), a transient growth controller is systematically designed and tested in both systems.
An economical and high-performance bioanalyzer, with no use of laptop computer, based on the use of TSPR1k23 biosensors was systematically designed, and validated experimentally for its high performance.
On the basis of previous reports on the importance of thienyl, furyl or phenol group substitution on 5H-indeno[1,2-b]pyridine skeleton, a new series of rigid 2-aryl-4(4′-hydroxyphenyl -5H-indeno[1,2-b]pyridine derivatives were systematically designed and synthesized.
For the target regions, primer pairs are systematically designed and, as the target regions are amplified by PCR, only the fragments with the right primer pairs are enriched.
We present data on 5 cyclic peptide bis(ZnII-dipicolylamines) which have been systematically designed as potential molecular biosensors for pyrophosphate (PPi).
