Chemical weed control is a significant agricultural concern, and reliance on a limited range of herbicide action modes has increased resistant weed species, many of which use C4 metabolism. As a result, the identification of novel herbicidal agents with low toxicity targeting C4 plants becomes imperative. An assessment was conducted on the impact of 3-cyanobenzoic acid on the growth and photosynthetic processes of maize (), a representative C4 plant, cultivated hydroponically over 14 days. The results showed a significant reduction in plant growth and notable disruptions in gas exchange and chlorophyll fluorescence due to the application of 3-cyanobenzoic acid, indicating compromised photosynthetic activity. Parameters such as the chlorophyll index, net assimilation (), stomatal conductance (), intercellular CO concentration (), maximum effective photochemical efficiency (F/F), photochemical quenching coefficient (q), quantum yield of photosystem II photochemistry (ϕ), and electron transport rate through PSII (ETR) all decreased. The /PAR curve revealed reductions in the maximum net assimilation rate () and apparent quantum yield (ϕ), alongside an increased light compensation point (LCP). Moreover, 3-cyanobenzoic acid significantly decreased the carboxylation rates of RuBisCo (V) and PEPCase (V), electron transport rate (), and mesophilic conductance (). Overall, 3-cyanobenzoic acid induced substantial changes in plant growth, carboxylative processes, and photochemical activities. The treated plants also exhibited heightened susceptibility to intense light conditions, indicating a significant and potentially adverse impact on their physiological functions. These findings suggest that 3-cyanobenzoic acid or its analogs could be promising for future research targeting photosynthesis.
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http://dx.doi.org/10.3390/plants14010001 | DOI Listing |
Plants (Basel)
December 2024
Laboratory of Plant Biochemistry, Department of Biochemistry, State University of Maringá, Maringá 87020-900, Brazil.
Chemical weed control is a significant agricultural concern, and reliance on a limited range of herbicide action modes has increased resistant weed species, many of which use C4 metabolism. As a result, the identification of novel herbicidal agents with low toxicity targeting C4 plants becomes imperative. An assessment was conducted on the impact of 3-cyanobenzoic acid on the growth and photosynthetic processes of maize (), a representative C4 plant, cultivated hydroponically over 14 days.
View Article and Find Full Text PDFSmall
December 2024
Institute of Functional Nano & Soft Materials (FUNSOM), Jiangsu Key Laboratory for Carbon-Based Functional Materials & Devices, Soochow University, Suzhou, Jiangsu, 215123, China.
The solution-derived non-stoichiometric nickel oxide (NiO) is a promising hole-injecting material for stable quantum dot light-emitting diodes (QLEDs). However, the carrier imbalance due to the misalignment of energy levels between the NiO and polymeric hole-transporting layers (HTLs) curtails the device efficiency. In this study, the modification of the NiO surface is investigated using either 3-cyanobenzoic acid (3-CN-BA) or 4-cyanobenzoic acid (4-CN-BA) in the QLED fabrication.
View Article and Find Full Text PDFInorg Chem
April 2009
Department of Chemistry, Nankai University, Tianjin 300071, PR China.
In our continuing efforts to explore the effects of ligand modifications on the structures and properties of their metal complexes, we studied the in situ [2 + 3] cycloaddition reactions of benzonitrile, o-phthalodinitrile, 3-cyanobenzoic acid, 4-cyanobenzoic acid with NaN(3) in the presence of Zn(II) and/or Co(II) salts under hydrothermal conditions, and obtained four new Co(II)-doped Zn(II)-tetrazole-benzoate coordination polymers with the formula of [Co(x)Zn(1-x)(L(m))(y)](n) [5-phenyl-1H-tetrazole (HL(1)) for 1, 2-(1H-tetrazol-5-yl)benzoic acid (H(2)L(2)) for 2, 3-(1H-tetrazol-5-yl)benzoic acid (H(2)L(3)) for 3, and 4-(1H-tetrazol-5-yl)benzoic acid (H(2)L(4)) for 4]. The structure of 1 shows a classical diamondoid net, while 2 and 3, take 2D layer structure with (4.6(2))(4.
View Article and Find Full Text PDFInorg Chem
June 2005
Department of Chemistry and State Key Laboratory for Physical Chemistry of Solid Surface, Xiamen University, Xiamen 361005, China.
A three-dimensional coordination polymer, [Mn3(OH)2Na2(3-cnba)6]n (1) (3-Hcnba = 3-cyanobenzoic acid), has been synthesized by the reaction of MnCl2, NaN3, and 3-Hcnba in water. Its crystal structure was determined by single-crystal X-ray diffraction. Magnetic studies show that the complex behaves as a three-dimensional metamagnet built from effective ferrimagnetic Mn(II) chains in which spin moments are linked by interactions in an AF-F-AF (F = ferromagnetic and AF = antiferromagnetic) sequence in the triangular magnetic repeating unit.
View Article and Find Full Text PDFJ Agric Food Chem
December 2002
Department of Agricultural Chemistry, Kyungpook National University, 1370, Sankyuk dong, Buk-gu, Daegu 702-701, Korea.
A modified Fenton reagent (Fe(3+)/H(2)O(2)) transformed the fungicide chlorothalonil within 60 min in aqueous solution at unadjusted pH. Transformation varied with ferric salt. Transformation was greatest with ferric nitrate and least when ferric sulfate was used.
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