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During stage 1 (days 0-100) when N stimulation effect reached a maximum, CO2 emissions from manure had positive relationships with labile C fraction indicators, including total sugars, soluble polyphenols, and lignin cinnamyl/vanillyl ratio regardless of N addition. N effect on manure decomposition was related to the C/N ratio and labile organic C content. During stage 2 (days 101-267), N effect shifted to inhibition, with CO2 emissions from manure negatively related to lignin vanillyl-units content. The magnitude of N inhibition increased linearly with the aromaticity of dissolved organic C, and was strengthened by nitrate in manure. Finally, N inhibition effect reached a maximum during stage 3 (days 268-365), increasing with higher aromatic C in manure. Critical factors for manure decomposition shifted from total sugars, soluble polyphenols, and lignin cinnamyl-units to recalcitrant lignin vanillyl-units and aromatic C fraction, which mediated the type and magnitude of N effect on decomposition.<br /><br /> Our results suggested that the potential for enhancing soil C sequestration with organic manures would magnify under combined application with N fertilizer in the long Characterization of unknown iodinated disinfection byproducts during chlorination/chloramination using ultrahigh resolution mass spectrometry.Iodinated disinfection byproducts (I-DBPs), formed from the reaction of disinfectant(s) with organic matter in the presence of iodide in raw water, have recently been focused because of their more cytotoxic and genotoxic properties than their chlorinated or brominated analogues. To date, only a few I-DBPs in drinking water have been identified. In this study, C18 solid phase extraction coupled with electrospray ionization ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry (ESI FT-ICR MS) was used to characterize unknown I-DBPs in chloraminated/chlorinated water spiked with iodide and humic substances. In total, 178 formulas for one-iodine-containing products, 13 formulas for two-iodine-containing products, and 15 formulas for one-chlorine and one-iodine-containing products were detected in the chloraminated water sample, while only 9 formulas for one-iodine-containing products and 6 formulas for one-chlorine and one-iodine-containing products were found in the chlorinated water sample. Most I-DBPs have corresponding chlorine-containing analogues with identical CHO compositions. As indicated by the modified aromaticity index (AImod), in the C18 extracts, more than 68% of the I-DBPs have aromatic structures or polycyclic aromatic structures.<br /><br /> This result demonstrates that the use of chloramination as an alternative disinfection method may lead to the formation of abundant species of I-DBPs in the presence of iodide. Thus, the suitability of adopting chloramination as an alternative disinfection method should be reevaluated, particularly when iodide is present in raw water.Zethrenes, extended p-quinodimethanes, and periacenes with a singlet biradical Researchers have studied polycyclic aromatic hydrocarbons (PAHs) for more than 100 years, and most PAHs in the neutral state reported so far have a closed-shell electronic configuration in the ground state. However, [http://allinno.com/news/166.html Seebio Photoinitiator] have revealed that specific types of polycyclic hydrocarbons (PHs) could have a singlet biradical ground state and exhibit unique electronic, optical, and magnetic activities. With the appropriate stabilization, these new compounds could prove useful as molecular materials for organic electronics, nonlinear optics, organic spintronics, organic photovoltaics, and energy storage devices. However, before researchers can use these materials to design new devices, they need better methods to synthesize these molecules and a better understanding of the fundamental relationship between the structure and biradical character of these compounds and their physical properties. Their biradical character makes these compounds difficult to synthesize.<br /><br /> These compounds are also challenging to physically characterize and require the use of various experimental techniques and theoretic methods to comprehensively describe their unique properties. In this Account, we will discuss the chemistry and physics of three types of PHs with a significant singlet biradical character, primarily developed in our group. These structures are zethrenes, Z-shaped quinoidal hydrocarbons; hydrocarbons that include a proaromatic extended p-quinodimethane unit; and periacenes, acenes fused in a peri-arrangement. We used a variety of synthetic methods to prepare these compounds and stabilized them using both thermodynamic and kinetic approaches. We probed their ground-state structures by electronic absorption, NMR, ESR, SQUID, Raman spectroscopy, and X-ray crystallography and also performed density functional theory calculations. [http://en.wikipedia.org/wiki/Photoresist 6-butyl-n-hydroxynaphthimide trifluoromethanesulfonic acid as a Catalyst in Organic Transformations] investigated the physical properties of these PHs using various experimental methods such as one-photon absorption, two-photon absorption, transient absorption spectroscopy, electrochemistry, and spectroelectrochemistry.