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1 e Si=C bonds are involved in an expanded pai-conjugated system.
2 the degree of pi-delocalization in a cyclic conjugated system.
3 modifying a heteroaromatic component in the conjugated system.
4 e delocalization stabilization of each fully conjugated system.
5 tor group that couples to the donor via a pi-conjugated system.
6 s introduced by chemical substitution on the conjugated system.
7 ncorporation of a histidine residue into the conjugated system.
8 ively, were perpendicular to the rest of the conjugated system.
9 ic side chains as well as a more extended pi-conjugated system.
10 tron-withdrawing CN groups stabilize the pai-conjugated system.
11 mine bonds thereby preserving the planar pai-conjugated system.
12 t reported tricyclic 5/5/5 ring with a fully conjugated system.
13 he diatropicity and paratropicity of the pai-conjugated system.
14 one, two, and three electrons added to its n-conjugated system.
15 stabilizing the aromatic character of the n-conjugated system.
16 nally diverse nitrogen-containing organic pi-conjugated systems.
17 molecular materials, including those from pi-conjugated systems.
18 pically looked at as nonpolar precursors for conjugated systems.
19 sses during an organic reaction involving pi conjugated systems.
20 tion-processed P3HT and more generally in pi-conjugated systems.
21 n refluxing toluene later produced the fully conjugated systems.
22 C(sp(3))-H bonds adjacent to heteroatoms or conjugated systems.
23 substrates, including aromatic compounds and conjugated systems.
24 al principles that can be applied to similar conjugated systems.
25 zarin core were employed to access the final conjugated systems.
29 it, capable of creating in S(1) an extended conjugated system and causing a substantial alternation
30 em, polyaniline (PANI) with pi-pi electronic conjugated system and effective photothermal efficiency
31 rins are stable molecules with a macrocyclic conjugated system and often peripheral substituents.
32 n from both the (3)pi,pi* manifold of the pi-conjugated system and the dpi Re --> pi* bpy-oligomer me
33 ty: those driven by formation of an extended conjugated system and those driven by selective silylati
34 derstanding the electronic properties of pai-conjugated systems and realizing high-performance molecu
35 nt from those of traditional closed-shell pi-conjugated systems, and thus they have many potential ap
39 a resonance dipolar structure of the [18]pai-conjugated system as the reduced congener with concomita
40 antly distorts the planarity of the extended conjugated system between the PLP ring and the internal
41 -endo process favorable thermodynamically in conjugated systems but also lowers its activation barrie
42 to dramatically enhance conductance in cross-conjugated systems by preventing reversal current format
43 During evaporative solution processing, pai-conjugated systems can assemble via various forms of int
44 Understanding the excited-state dynamics in conjugated systems can lead to their better utilization
45 f 52 larger molecules (including challenging conjugated systems, carbohydrates, small drugs, amino ac
46 tes a cascade reaction to yield a complex pi-conjugated system containing phthalide and indene subuni
48 alc multiplied by the number of atoms in the conjugated system, DeltaEcalcT, and the sum of the NICS
49 h makes it an interesting building block for conjugated systems designed for organic electronics.
50 ctors governing rotational barriers in cross-conjugated systems exhibiting correlated molecular motio
51 ering strategies based on donor-acceptor pai-conjugated system facilitates expedient molecular packin
52 ctance properties of pi-conjugated and sigma-conjugated systems have been well-studied, little is kno
53 ke molecules with two orthogonally placed pi-conjugated systems have in recent years attracted signif
54 addition reactions of oxygen nucleophiles to conjugated systems, have traditionally received much les
57 ical character for a variety of extended pai-conjugated systems, including some salient recent exampl
58 emarkable features: (i) Considering the 28pi-conjugated system, instantaneous and site-selective Zn(I
59 ocalize over the entire length of the longer conjugated systems; instead they are polarons occupying
60 we demonstrate that the extension of the pi-conjugated system is an efficient way to improve the hig
61 ent a class of fluorophores in which the pai-conjugated system is rigidified and stabilized by a boro
62 ion within the designed extended helical pai-conjugated systems is a crucial factor to reach chemical
64 ion of o-carborane clusters into extended pi-conjugated systems led to 22-70% enhancement of their re
65 hat the stability and photo-physics of these conjugated systems may be ascribed to their cationic nat
68 en-emitting BBB, gBBB, and, by expanding the conjugated system of the Bodipy core at alpha-position,
69 anding of charge distribution in extended pi-conjugated systems of different topologies, and concomit
70 system allows for increased stability of the conjugated system relative to linear analogues due to th
75 on leads to dearomatization of the porphyrin conjugated system, thereby favoring protonation at the m
76 very different from those in typical linear conjugated systems: These systems have a band of excited
77 these design strategies are well explored in conjugated systems, they have not been implemented with
78 ymmetric charge transfer, from the ends of a conjugated system to the middle, or vice versa, upon exc
79 ceeding the olefination establishes a highly conjugated system to which a salt-free Wittig reaction a
84 to the delocalized energy-minimum state of a conjugated system, using our newly developed block-local
87 tion with an increase in the size of the pai-conjugated system was observed, reaching 80 GM for the n
88 tions containing two structurally related pi-conjugated systems were studied to probe pi-pi interacti
89 ugated, conjugation-interrupted and linearly conjugated systems were synthesized and characterized.
91 plications; however, many NIR dyes are large conjugated systems which frequently have issues with sta
92 erview the existing literature on chiral pai-conjugated systems whose thin films have been characteri
94 damental building block for the design of pi-conjugated systems with low band gap and open-shell bira