ライフサイエンスコーパス: conjugated system

1 e delocalization stabilization of each fully conjugated system.

2 tor group that couples to the donor via a pi-conjugated system.

3 s introduced by chemical substitution on the conjugated system.

4 ncorporation of a histidine residue into the conjugated system.

5 ively, were perpendicular to the rest of the conjugated system.

6 ic side chains as well as a more extended pi-conjugated system.

7 the degree of pi-delocalization in a cyclic conjugated system.

8 modifying a heteroaromatic component in the conjugated system.

9 molecular materials, including those from pi-conjugated systems.

10 pically looked at as nonpolar precursors for conjugated systems.

11 zarin core were employed to access the final conjugated systems.

12 sses during an organic reaction involving pi conjugated systems.

13 tion-processed P3HT and more generally in pi-conjugated systems.

14 nally diverse nitrogen-containing organic pi-conjugated systems.

15 n refluxing toluene later produced the fully conjugated systems.

16 was rotated perpendicular to the rest of the conjugated system (7).

17 Thus, for this class of pi-conjugated system, an unprecedented off-pathway aggregat

18 em, polyaniline (PANI) with pi-pi electronic conjugated system and effective photothermal efficiency

19 rins are stable molecules with a macrocyclic conjugated system and often peripheral substituents.

20 n from both the (3)pi,pi* manifold of the pi-conjugated system and the dpi Re --> pi* bpy-oligomer me

21 ty: those driven by formation of an extended conjugated system and those driven by selective silylati

22 nt from those of traditional closed-shell pi-conjugated systems, and thus they have many potential ap

23 e C-Zr directions, indicating that the whole conjugated systems are nonetheless involved.

24 Influencing the communication within a conjugated system as diphenylacetylene is a challenging

25 antly distorts the planarity of the extended conjugated system between the PLP ring and the internal

26 -endo process favorable thermodynamically in conjugated systems but also lowers its activation barrie

27 Understanding the excited-state dynamics in conjugated systems can lead to their better utilization

28 tes a cascade reaction to yield a complex pi-conjugated system containing phthalide and indene subuni

29 tructural, and electronic properties of such conjugated systems containing CBD.

30 alc multiplied by the number of atoms in the conjugated system, DeltaEcalcT, and the sum of the NICS

31 h makes it an interesting building block for conjugated systems designed for organic electronics.

32 ctance properties of pi-conjugated and sigma-conjugated systems have been well-studied, little is kno

33 ke molecules with two orthogonally placed pi-conjugated systems have in recent years attracted signif

34 addition reactions of oxygen nucleophiles to conjugated systems, have traditionally received much les

35 ct of the tag increases with the size of the conjugated system in the order Benz < Naph < Anth.

36 Stacking interaction of the conjugated systems in the dimeric complexes contributes

37 emarkable features: (i) Considering the 28pi-conjugated system, instantaneous and site-selective Zn(I

38 ocalize over the entire length of the longer conjugated systems; instead they are polarons occupying

39 we demonstrate that the extension of the pi-conjugated system is an efficient way to improve the hig

40 ion of o-carborane clusters into extended pi-conjugated systems led to 22-70% enhancement of their re

41 Because of the extended pi-electron-conjugated system of carotenoid molecules, the cation ra

42 consequence of the expansion of the existing conjugated system of double bonds.

43 anding of charge distribution in extended pi-conjugated systems of different topologies, and concomit

44 system allows for increased stability of the conjugated system relative to linear analogues due to th

45 system allows for increased stability of the conjugated system relative to linear analogues.

46 on leads to dearomatization of the porphyrin conjugated system, thereby favoring protonation at the m

47 very different from those in typical linear conjugated systems: These systems have a band of excited

48 ymmetric charge transfer, from the ends of a conjugated system to the middle, or vice versa, upon exc

49 ceeding the olefination establishes a highly conjugated system to which a salt-free Wittig reaction a

50 ort dominates at all temperatures for the pi-conjugated system (type II).

51 Two azo-ene-butadiyne conjugated systems undergo CuCl-mediated cyclization to

52 to the delocalized energy-minimum state of a conjugated system, using our newly developed block-local

53 The elongation of the pi-conjugated system via additional ethenylene linker resul

54 r phycocyanobilins), which have an extensive conjugated system, vulnerable to autoxidation.

55 tions containing two structurally related pi-conjugated systems were studied to probe pi-pi interacti

56 damental building block for the design of pi-conjugated systems with low band gap and open-shell bira

57 new route for constructing purine-nucleoside-conjugated systems with two newly formed C-N bonds.