Studies on photocrosslinkable polymers having bromo-substituted pendant cinnamoyl group

Balaji, R.; Grande, Daniel; Nanjundan, S.

doi:10.1016/s1381-5148(03)00031-2

Cited by 27 publications

(16 citation statements)

References 21 publications

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“…Chalcones and their analogues are used as potential therapeutic agents in diseases of the cardiovascular system (Opletalova et al, 2003). Photo-cross-linkable polymers having the chalcone moiety act as negative photoresist materials used in a wide variety of applications (Balaji et al, 2003). Chalcones are also used in designing effective second-order non-linear optical materials (Zhao et al, 2000).…”

Section: Commentmentioning

confidence: 99%

3-(3-Hydroxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one

Moorthi¹,

Chinnakali²,

Nanjundan³

et al. 2005

Acta Cryst E

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Section: Commentmentioning

confidence: 99%

3-(3-Hydroxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one

Moorthi¹,

Chinnakali²,

Nanjundan³

et al. 2005

Acta Cryst E

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“…For related literature, see: Arty et al (2000); Balaji et al (2003); Batt et al (1993); De Leon et al (2003); Dimmock et al (1999); Harrison et al (2006); Modzelewska et al (2006); Ng et al (2006); Opletalova & Sedivy (1999); Opletalova et al (2003); Patil et al (2007); Sogawa et al (1994); Won et al (2005); Yathirajan et al (2006); Zhao et al (2000).…”

Section: Related Literaturementioning

confidence: 99%

(2E)-3-(5-Bromo-2-thienyl)-1-(4-hydroxyphenyl)prop-2-en-1-one

Narayana

Lakshmana

Sarojini³

et al. 2007

Acta Cryst E

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Key indicators: single-crystal X-ray study; T = 173 K; mean (C-C) = 0.003 Å; R factor = 0.031; wR factor = 0.066; data-to-parameter ratio = 15.5.Geometric parameters of the title compound, C 13 H 9 BrO 2 S, a chalcone derivative, are in the usual ranges. The C C double bond is trans configured. The molecule is essentially planar (r.m.s. deviation for all non-H atoms = 0.069 Å ). The crystal packing is stabilized by an O-HÁ Á ÁO hydrogen bond. Related literature ExperimentalCrystal data

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“…4 The chalcone core crystals nd a place in optics, communications, liquid crystals and frequency modulation. [6][7][8] The chalcone nonlinear optical materials are expected to be dynamic for optical communication and opto-electronics because of their applications in highspeed and high-density data processing. [9][10][11] Second order nonlinear optical materials were used in optical switching, frequency conversion and electro-optical applications.…”

Section: Introductionmentioning

confidence: 99%

Substitution effect on chalcone based materials for corrosion and photocrosslinking applications

Vanaraj

Anandhi²,

Kannan

2015

RSC Adv.

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Three different substituted novel chalcone based materials namely (E)-3-(4-(benzyloxy)phenyl)-1-(4-hydroxyphenyl)prop-2-en-1-one (chalcone I), (E)-1-(4-(benzyloxy)phenyl)-3-(4-hydroxyphenyl)prop-2-en-1-one (chalcone II) and (E)-1,3-bis(4-(benzyloxy)phenyl)prop-2-en-1-one (chalcone III) were designed and synthesized by a standard Claisen-Schmidt condensation reaction. The different surface morphologies of these materials were obtained from SEM (Scanning Electron Microscopy) analysis.Single crystal XRD studies of chalcone III indicate a monoclinic system with a space group of P2 1 /c. Thermal studies such as TGA, DSC and HOPM revealed good thermal stability, crystallinity and phase changing properties of material III. The HOMO, LUMO and bandgap energies of these three materials were calculated by theoretical (DFT) calculations. The electrochemical analysis involves Tafel plots and cyclic voltammetry studies to demonstrate high corrosion inhibition percentage and oxidation-reduction behaviour of materials I, II and III. Dissimilar photocrosslinking time of all three materials was obtained from micro photo-reactor and UV-visible spectrophotometry. The comparative and structural linearity statement reveals the outline view property of the similar chalcone families.

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Studies on photocrosslinkable polymers having bromo-substituted pendant cinnamoyl group

Cited by 27 publications

References 21 publications

3-(3-Hydroxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one

3-(3-Hydroxyphenyl)-1-(4-methoxyphenyl)prop-2-en-1-one

(2E)-3-(5-Bromo-2-thienyl)-1-(4-hydroxyphenyl)prop-2-en-1-one

Substitution effect on chalcone based materials for corrosion and photocrosslinking applications

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