Temperature-Based Fan Speed Optimization Strategy

As energy efficiency and indoor comfort increasingly become key standards in modern residential and office environments,research on intelligent fan speed control systems has become particularly important.This study aims to develop a temperature-feedback-based fan speed optimization strategy to achieve higher energy efficiency and user comfort.Firstly,by analyzing existing fan speed control technologies,their main limitations are identified,such as the inability to achieve smooth speed transitions.To address this issue,a BP-PID speed control algorithm is designed,which dynamically adjusts fan speed based on indoor temperature changes.Experimental validation demonstrates that the designed system can achieve smooth speed transitions compared to traditional fan systems while maintaining stable indoor temperatures.Furthermore,the real-time responsiveness of the system is crucial for enhancing user comfort.Our research not only demonstrates the feasibility of temperature-based fan speed optimization strategies in both theory and practice but also provides valuable insights for energy management in future smart home environments.Ultimately,this research outcome will facilitate the development of smart home systems and have a positive impact on environmental sustainability.

Synthesis and reactivity of cobalt dinitrogen complex supported by nonsymmetrical pincer ligand

A nonsymmetrical PNN pincer ligand[6-(^(t)Bu_(2)PNH)C_(5)H_(4)N-2-(3-Mes)C_(3)H_(2)N_(2)]and its corresponding cobalt-N_(2)complex were synthesized and characterized.By the stoichiometric reaction of the PNN ligand lithium salt with CoCl_(2),the complex 3,(PNN)CoCl,was obtained.Then,reduction of 3 with NaBHEt3under a dinitrogen atmosphere yielded complex 5,(PNN)Co(Ⅰ)(η^(1)-N_(2)).Single-crystal X-ray analysis,IR spectrum,and DFT calculations revealed that the dinitrogen in 5 was only weakly reduced by the cobalt center.The reactions of 5 with carbon monoxide and 2,6-dimethylphenyl isocyanide gave carbonyl and isocyanide complexes 6 and 7 with the release of N_(2),respectively.Furthermore,these cobalt complexes,especially complex 5,demonstrated the capacity to convert dinitrogen to N(TMS)_(3)with moderate efficiency.

固氮反应中的凝聚态化学

氮是构成生命和物质世界不可或缺的元素,发展高效的转化方法将氮气分子转变为具有各种功能的含氮化合物,具有重要的经济价值和科学意义。氮气分子的活化转化是化学学科永恒的课题,而凝聚态化学的研究方法和多层面认识对固氮研究具有深刻意义。本文列举了一些固氮化学中的凝聚态现象,从均相溶液固氮、多相合成氨以及氮气/氧气多能耦合转化等三方面,讨论了目前固氮化学领域中存在的关键科学问题,期望启发更多学者从凝聚态化学角度思考固氮化学反应本质,为解决相关问题提供更多新的思路。

Light-Driven Dinitrogen Activation with Transition Metal Complexes:Mechanisms and Applications

Comprehensive Summary,The Haber-Bosch process,which is used for ammonia(NH3)synthesis,requires vast amounts of energy,accounting for approximately 1%—2%of the world's annual energy consumption.Therefore,researchers in both industry and academia are interested in developing sustainable and environmentally friendly methods for synthesizing nitrogenous compounds at ambient conditions using renewable energy sources such as visible light.While several examples of thermal activation of dinitrogen molecules have been demonstrated using various transition metals and ligand frameworks,the use of light to weaken or split the strong N—N bond has been less explored.This article presents an overview of molecular complexes capable of dinitrogen photocleavage and provides mechanistic insights into the photoactivation process through experimental and theoretical studies.We believe this review will provide readers with an in-depth understanding of the current state-of-the-art and future research perspectives,particularly in the use of visible light for dinitrogen activation and transformation.

Advances in electrochemical transformation of N_(2)using molecular catalysts

The conversion of N_(2)to NH_(3)holds great importance due to the essential role of NH_(3)in fertilizer production,energy storage and the synthesis of key industrial chemicals.Development of novel methods for N_(2)transformation is a worthwhile goal and researchers have turned their attention to electrochemical N_(2)reduction as a potentially sustainable solution.The development of molecular electrocatalysts has gained considerable momentum over the last decades,and this review focuses on the advances and challenges in the field of molecular electrochemical nitrogen fixation and aims to inspire further research into the realm of nitrogen fixation chemistry from an electrochemical perspective.

Synthesis and structural analysis of titanium-μ-dinitrogen complex supported by di-anionic guanidinate ligands

The synthesis,characterization,and theoretical studies of titanium-μ-N_(2) complexes with di-anionic guanidinate ligands were reported as the first example of its kind.Thus,with(Me_(3)Si)_(2)N-guanidinate ligands,the mono-anionic guanidinate-supported titanium-μ-N2complex 1 was obtained.Then,reduction of 1 with potassium afforded the di-anionic guanidinate-supported titanium-μ-N_(2) complex 2 via cleavage of one N–Si bond of the(Me3Si)2N substituents in 1,changing the guanidinate ligands automatically from mono-anionic to di-anionic and remarkably lengthening the bond length of theμ-N_(2).Characteristic studies and DFT calculations were performed to reveal that the di-anionic guanidinate ligands stabilized the geometry of 2 and increased the charge density on the bridging dinitrogen.

One-Electron Reduction of Constrained and Unsymmetric Diiron Dinitrogen Complexes

Iron sites in both nitrogenase enzymes and chemical catalysts for N_(2) fixation are typically at constrained distances and angles.Herein,we report a one-electron reduction reaction realized by constrained diiron dinitrogen cores.Using the semicircular bis(β-diketiminate)ligand,a series of diiron dinitrogen complexes were synthesized,in which the N_(2) groups were allowed to bind with Fe-Ct_(N2)-Fe angles ranging from 154°to 158°(Ct_(N2)=centroid of N_(2)).One-electron reduction of complex 2a[LFe(μ-N_(2))Fe(Et_(2)O)]gave dimer product 3a[LFe(μ-N_(2))FeK]_(2)(μ-N_(2))or monomer 3b[LFe(μ-N_(2))Fe(DMAP)K].Based on superconducting quantum interference device measurements and density functional theory calculations,2a,3a,and 3b exhibited ground spin states of S=3,S=5,and S=5/2,respectively.In addition,complex 3 underwent N_(2)derivatization via a silylation pathway followed by an acidic cleavage to yield N_(2)H_(4)as the product.

Direct and chlorine-free synthesis of phosphafluorenes or their oxides from white phosphorus

The known methods for the preparation of acylphosphine oxides and polyfluorobenzene-substituted triarylphosphines need to utilize PCl_(3),while the chlorine-free methods are not reported.In this work,we report a chlorine-free method by one-pot three-component reaction of white phosphorus(P_(4)),dilithio reagents,and acyl chlorines or polyfluorobenzenes for the synthesis of biphenyl-based acylphosphine oxides and phosphines.This reaction is green and environmentally friendly compared with the traditional method,because it avoids the use of Cl_(2) and the discharge of a large amount of waste gas and waste acid.These two products have potential applications as photoinitiators in photopolymerization or as organophosphorus ligands in catalytic reactions.

Phosphafluorenyl lithiums:direct synthesis from white phosphorus,structure and diversified synthons

While rich chemistry of phospholyl anions is discovered,phosphafluorenyl anions are only proposed as the critical intermediates for the synthesis of phosphafluorenes.In this article,we reported the direct synthesis of phosphafluorenyl lithiums from white phosphorus(P_(4))through direct P-C bond formation.The reaction between P4 and biphenyl dilithio reagents efficiently afforded phosphafluorenyl lithiums,which were further used to synthesize different kinds of organophosphorus compounds.The aggregation states of phosphafluorenyl lithiums were investigated for the first time.Mechanistic studies by DFT calculations revealed a cooperative nucleophilic attack of two C−Li bonds on P_(4)molecule.

Dinitrogen Functionalization Affording Structurally Well-Defined Cobalt Diazenido Complexes

Cobalt-bis(dinitrogen)complexes[LCo(N_(2))_(2)]−(3,4)with simple and commercially available bidentate phosphine ligands(L:Cy_(2)PCH_(2)CH_(2)PCy_(2))were synthesized and structurally characterized.Further N2 functionalization by treating the complex 3b with i Pr_(3)SiCl afforded the first structurally characterized cobalt diazenido complex 5.These complexes 3–5 were found to be effective catalysts for the transformation of N2 into N(SiMe_(3))_(3).The electronic structure of the cobalt diazenido complex 5 is supported by quantum computational calculations based on stateof-the-art energy decomposition analysis(EDA)in conjunction with the natural orbitals for chemical valence(NOCV)method.

Dinitrogen Activation of Cyclopentadienyl-Phosphine–Iron Complexes of Three Different Valences

A series of structurally well-defined iron-dinitrogen complexes(LFe-N2)bearing cyclopentadienylphosphine ligands(L)were synthesized and analyzed by single-crystal X-ray structural analysis,IR/Raman spectra,magnetometry,Mössbauer spectroscopy,and elemental analysis.The conversion relationship and the change of the spin states among the iron complexes with different valences were studied in detail.

Rare-Earth Metal Boroxide with Formal Triple Metal-Oxygen Orbital Interaction:Synthesis from B(C_(6)F_(5))_(3)·H_(2)O and Radical-Anion Ligated Rare-Earth Metal Amides

Rare-earth metal boroxides are not only rare and of great synthetic challenge but also important theoretically due to their unrevealed bonding characteristics.In this paper,we report the synthesis,characterization,and bonding characteristics of the 4f-block metal boroxide complexes ^(Mes)DAD_(2)LuOB(C_(6)F_(5))X(4-Lu,X=C_(6)F_(5);5-Lu,X=NC_(13)H_(10))with two chelating radical-anionic 1,4-diazabutadiene(DAD)ligands.The synthesis of 4-Lu or 5-Lu involved three steps,during which the radical-anionic DAD ligands could be kept stable:(1)the reaction of LuCl_(3),^(Mes)DAD,and potassium graphite(KC8)afforded the diradical rare-earth metal chloride ^(Mes)DAD_(2)LuCl·tetrahydrofuran(THF)(1-Lu);(2)the salt metathesis of 1-Lu with two alkali metal amides gave lutetium bis(diazabutadiene)amides 2-Lu or 3-Lu,respectively;and(3)2-Lu or 3-Lu reacted with B(C_(6)F_(5))_(3)·H_(2)O,resulting in the formation of rare-earth metal boroxides 4-Lu or 5-Lu.The radical-anionic nature of DAD ligands in these complexes were proven by their bond lengths and coordination modes in single-crystal structures.DFT calculations clearly show the bonding of 4-Lu can be divided into three major types of Lu-O orbital interactions,which can be categorized asσ-donation,π-donation,and d-π-conjugation.The triple Lu-O orbital interactions cooperatively make a Lu-O single bond and contribute to the linear Lu-O-B structure.