钱旭红

钱旭红，男，1962年2月19日生于江苏宝应，长江学者、博导、教授、“973”首席科学家、中国工程院院士、国家自然科学基金化学部咨询委员、英国皇家化学会会士、德国洪堡基金会学术大使。曾任华东理工大学校长。华东师范大学校长、党委副书记。^[3][4][1]

钱旭红1978年至1982年就读于华东化工学院石油化工系获得学士学位，1982年至1985年继续留校攻读精细化工系硕士学位。1988年获得博士学位。^[2]1989年至1990年，钱旭红任美国拉玛大学副研究员。^[5]2007年-2008年，钱旭红任亚洲及太平洋化工联盟主席。2011年12月钱旭红当选中国工程院院士。2014年，钱旭红兼任中国工程院化工、冶金与材料工程学部常委。^[5]曾经先后入选或获得国家百万千万人才工程、长江学者奖励计划、国家杰出青年基金、国家“973”项目首席科学家、上海市科技精英等。^[1]钱旭红主要从事绿色农药及功能染料研究及应用开发。作为第一、第二发明人获中国发明专利授权20余项，获美、欧、日等外国专利授权15项；发表论文350余篇，他引8000余次，10篇代表论文他引2500余次。^[1]

1994年，钱旭红获得国家教委科学技术进步奖一等奖，1998年获得中国高校科学技术奖一等奖，2008年获得国家科学技术进步奖二等奖，2022年获得高等教育（本科）国家级教学成果奖一等奖。^[2]

钱旭红1978年至1982年就读于华东化工学院石油化工系获得学士学位，1982年至1985年继续留校攻读精细化工系硕士学位。1988年获得博士学位。^[2]

钱旭红1989年-1990年担任美国拉玛大学副研究员，紧接着成为德国维尔茨堡大学洪堡基金博士后。1992年至2000年任华东理工大学讲师、副教授、教授，任精细化工学科主任、药物化工所所长、校长助理，1996年到2000年任华东理工大学副校长。2000年-2004年为大连理工大学长江学者特聘教授。2004年7月至2015年3月任华东理工大学校长、党委副书记。^[1]

2007年-2008年，钱旭红任亚洲及太平洋化工联盟主席。2011年12月钱旭红当选中国工程院院士，2014年兼任中国工程院化工、冶金与材料工程学部常委。自2018年1月起担任华东师范大学校长、党委副书记。曾经先后入选或获得国家百万千万人才工程、长江学者奖励计划、国家杰出青年基金、国家“973”项目首席科学家、上海市科技精英等。中国化工学会副理事长、英国皇家化学会会士、英国巴斯大学名誉教授、英国女王大学荣誉博士。^[1]担任《Chinese Chemical Letters》主编，J. Agr. Food Chem., Pestic. Biochem. Phys., J. Pestc. Sci.等国际期刊顾问编委，钱旭红还曾经兼任国家自然科学基金化学部咨询委员会委员、德国洪堡基金会学术大使等。^[1]2024年1月10日，钱旭红获“首届上海市科创教育年度人物”称号^[6]

钱旭红主要从事绿色农药及功能染料研究及应用开发。开发出沙星类药物核心中间体多氟fú芳酸等的绿色高效制备关键技术；创制新机制、性能独特的顺硝烯杂环类烟碱杀虫剂和多氟烷wán氧类植物健康激活剂等绿色农药，三个创制品种（哌pài虫啶dìng、环氧虫啶、氟唑活化酯zhǐ）获得登记；创制分子识别传感和检测分离一体化的萘nài酰亚胺等芳杂环类荧光染料；提出并实施化学生物技术与工程的概念和方法。作为第一完成人，获得国家教育部科技进步一等奖3项，上海市自然科学一等奖1项和国家科技进步二等奖1项。作为第一、第二发明人获中国发明专利授权20余项，获美、欧、日等外国专利授权15项；发表论文350余篇，他引8000余次，10篇代表论文他引2500余次。^[1]

 其研究主要集中在荧光传感器与新机制抗癌先导，包括以下内容：

荧光传感器：由萘、萘酰亚胺、香豆素、氟硼吡咯、聚合物衍生的高选择性过渡及重金属离子(汞、铜、锌、银、钯等)荧光传感器；某些阴离子、酶的荧光传感器；以及其它的荧光探针、荧光标记。^[4]

抗癌先导：由硫化合物、噻类芳香杂环、羰tāng酰xiān亚胺、萘酰亚胺、萘内酰胺、苯并吲哚duǒ酚嗪qín、吖啶、苊è萘醌kūn、苊萘吡咯羰腈jīng、酞菁等衍生的抗癌试剂，BCL蛋白与细胞调亡剂，拓扑异构酶抑制剂，光动力治疗剂，色素的药物化学(抗肿瘤先导、DNA嵌入剂、细胞调亡剂)。^[4]

其研究主要集中在芳香杂环或氟化合物衍生的农药先导，包括以下内容：

昆虫调节剂与杀虫剂先导：针对几丁质合成抑制、蜕皮激动、海藻糖酶抑制、拒食、飞行调控的昆虫生长调节剂与行为调节剂，烟碱受体激动类杀虫剂。^[4]  

新杂环化合物：主要有具有农药活性的氟化合物、氟烷氧基化合物、硫化合物、恶二唑、噻二唑、哒嗪酮tóng、新烟碱、环亚胺、二芳酰基肼jǐng等。^[4]

其研究主要集中在人工核酸酶、细胞激活剂和生物转化，包括以下方面：

人工核酸酶：由萘酰亚胺、硫杂环衍生的人工光核酸酶，人工核酸水解酶，DNA切断剂；生物制备过程中转基因物质的去除。^[4]

细胞激活剂：由茉莉酮酸酯、苯并噻二唑等衍生的细胞激活剂；用于人参、紫杉烷、灵芝的次生代谢物的增产与调控。^[4]

生物转化：酵母、植物细胞催化或导致的刚性芳香与杂环化合物的硝基及酮立体选择性还原，化学选择性还原。^[4] 

ORG. LETT.-2006-3721: A series of polyamide receptor based PET fluorescent sensor molecules: Positively cooperative Hg2+ ion binding with high sensitivity

ORG. LETT. 2005-3029: Colorimetric and ratiometric fluorescent chemosensor with a large red-shift in emission: Cu（Ⅱ）-only sensing by deprotonation of secondary amines as receptor conjugated to naphthalimide fluorophore

ORG. LETT.-2005-889: Ratiometric and selective fluorescent sensor for Cu-Ⅱ based on internal charge transfer (ICT)

ORG. LETT. 2004-2757: Novel fluorescent pH sensors based on intramolecular hydrogen bonding ability of naphthalimide (SS)

J. ORG. CHEM.-2006-4308: Detecting Hg2+ ions with an ICT fluorescent sensor molecule: Remarkable emission spectra shift and unique selectivity

J. ORG. CHEM.-2007-3554: Ratiometric and highly selective fluorescent sensor for cadmium under physiological pH range: A new strategy to discriminate cadmium from zinc

CHEM. COMMUN.-2006-109: Two regioisomeric and exclusively selective Hg（Ⅱ） sensor molecules composed of a naphthalimide fluorophore and an o-phenylenediamine derived triamide receptor

CHEM. COMMUN.-2005-239: A new class of long-wavelength fluorophores: strong red fluorescence,convenient synthesis and easy derivation

CHEM. COMMUN.-2001-2656: Intramolecular aromatic 1,5-hydrogen transfer in preparation of oxacyclic naphthalic anhydride via unusual Pschorr cyclisation

NEW J. CHEM.-2003-337: A polyamidoamine dendrimer with peripheral 1,8-naphthalimide groups capable of acting as a PET fluorescent sensor for metal cations

NEW J. CHEM.-2002-920: Novel heterogeneous PET fluorescent sensors selective for transition metal ions or protons: polymers regularly labelled with naphthalimide

J. AM. CHEM. SOC.-2004-2272: A highly selective and sensitive fluorescent chemosensor for Hg2+ in neutral buffer aqueous solution

KIDNEY INTERNATIONAL-2004-2279: Fluorescent imaging of acute mercuric chloride exposure on cultured human kidney tubular epithelial cells

CHEM. RES. TOⅪC.-2005-1814: Visible study of mercuric ion and its conjugate in living cells of mammals and plants

CHEMBIOCHEM-2007-113: Novel Bcl-2 inhibitors: Discovery and mechanism study of small organic apoptosis-inducing agents (SS)

J. MATER. CHEM. -2005-2836: A pH-resistant Zn（Ⅱ） sensor derived from 4-aminonaphthalimide: design,synthesis and intracellular applications

MOL. CANCER THER.-2007-484: R16,a novel amonafide analogue,induces apoptosis and G2-M arrest via poisoning topoisomerase Ⅱ (SS)

BIOORG. MED. CHEM. LETT.-2006-1562: Synthesis and evaluation of novel 8-oxo-8H-cyclopenta[a]acenaphthylene-7-carbonitriles as long-wavelength fluorescent markers for hypoxic cells in solid tumor

BIOORG. MED. CHEM. LETT.-2005-5909: Novel synthetic isoquinolino[5,4-ab]phenazines: Inhibition toward topoisomerase I,antitumor and DNA photo-cleaving activities

BIOORG. MED. CHEM. LETT.-2005-4864: Novel thiazonaphthalimides as efficient antitumor and DNA photocleaving agents: Effects of intercalation,side chains,and substituent groups (SS)

BIOORG. MED. CHEM. LETT.-2005-4864: Synthesis,antitumor evaluation and DNA photocleaving activity of novel methylthiazonaphthalimides with aminoalkyl side chains (SS)

BIOORG. MED. CHEM. LETT.-2005-1139: Five-member thio-heterocyclic fused naphthalimides with aminoalkyl side chains: intercalation and photocleavage to DNA (SS)

BIOORG. MED. CHEM. LETT.-2003-5427: Novel naphthalimide hydroperoxide photonucleases: The role of thiocyclic-fused area and the difference in spectra,photochemistry and photobiological activity (SS)

BIOORG. MED. CHEM.-2007-1356: Novel antitumor agent family of 1H-benzo[c,d]indol-2-one with flexible basic side chains: Synthesis and biological evaluation (SS)

BIOORG. MED. CHEM.-2006-6962：Acenaphtho[1,2-b]pyrrole derivatives as new family of intercalators: Various DNA binding geometry and interesting antitumor capacity (SS)

BIOORG. MED. CHEM.-2006-4639: Design,synthesis,and antitumor evaluation of novel acenaphtho[1,2-b]pyrrole-carboxylic acid esters with amino chain substitution (SS)

BIOORG. MED. CHEM. -2005-3149: Novel heterocyclic family of phenyl naphthothiazole carboxamides derived from naphthalimides: synthesis,antitumor evaluation,and DNA photocleavage (SS)

BIOORG. MED. CHEM.-2005-1615: Thio-heterocylic naphthalimides with aminoalkyl side chains: novel alternative tools for photodegradation of genomic DNA without impairment on bioactivities of proteins (SS)

TETRAHEDRON LETT.-2005-6289: A proton sponge-based fluorescent switch

TETRAHEDRON LETT.-2004-3969: A novel chromatism switcher with double receptors selectively for Ag+ in neutral aqueous solution: 4,5-diaminoalkeneamino-N-alkyl-1,8-naphthalimides

TETRAHEDRON LETT.-2003-2087: Novel highly efficient fluoroionophores with a peri-effect and strong electron-donating receptors: TICT-promoted PET and signaling response to transition metal cations with low background emission

TETRAHEDRON LETT.-2003-795: Promoting effects of the hydroxymethyl group on the fluorescent signaling recognition of anions by thioureas

TETRAHEDRON LETT.-2002-2991: 4-Amino-1,8-dicyanonaphthalene derivatives as novel fluorophore and fluorescence switches: efficient synthesis and fluorescence enhancement induced by transition metal ions and protons

TETRAHEDRON LETT.-2002-2995: Synthesis and properties of benzothioxanthene dicarboximide hydroperoxide: an efficient 'time-resolved' DNA photocleaver with long-wavelength (SS)

TETRAHEDRON LETT.-2001-6175: N-aroyloxynaphthalimides as novel highly efficient DNA photocleavers: substituent effects

TETRAHEDRON LETT.-2000-7711: Novel and highly efficient DNA photocleavers: hydroperoxides of heterocyclic-fused naphthalimides

TETRAHEDRON-2005-11895: Novel DNA bis-intercalators of isoquinolino[4,5-bc]acridines: design,synthesis and evaluation of cytotoxic activity

TETRAHEDRON-2005-8717: Synthesis,antitumor and DNA photocleaving activities of novel naphthalene carboxamides: effects of different thio-heterocyclic rings and aminoalkyl side chains (SS)

TETRAHEDRON-2005-6634: Synthesis of thiazo- or thiadiazo- naphthalene carboxamides via mercuric intermediates and their antitumor and DNA photocleavage activities (SS)

TETRAHEDRON-2006-10117: Exploiting the deprotonation mechanism for the design of ratiometric and colorimetric Zn2+ fluorescent chemosensor with a large red-shift in emission

DYES PIGMENTS-2002-247: Synthesis and properties of oligonucleotides containing fluorescent ethenodeoxyadeno sine and ethenodeoxycytidine

DYES PIGMENTS-2001-51: Absorption and fluorescence spectral properties of tetra (fluoroalkoxy) metallophthalocyanines (FF)

DYES PIGMENTS-2001-43: Oxazolonaphthalimides and their hydroperoxides: photophysical and photobiological properties

DYES PIGMENTS-2004-9: Benzothioxanthene dyes as fluorescent label for DNA hybridization: synthesis and application (SS)

DYES PIGMENTS-2004-17: Synthesis and peroxidase-staining properties of novel water soluble polyhydroxylalkyl benzidine dyes

J. FLUORINE CHEM.-2002-161: Synthesis and photosensitizing properties of fluoroalkoxyl phthalocyanine metal complexes (FF)

J. FLUORINE CHEM.-2000-69: Synthesis of fluorine-containing oxazolonaphthalimide hydroperoxides as DNA photocleavers (FF)

CHINESE J. ORG. CHEM.1997-329: Synthesis and characterizations of the dye sensitized photooxygenation products and the heterocycles of naphthofuran derivatives

CHINESE J. ORG. CHEM.-1997-428: Synthesis,characterization and DNA intercalation of a furonaphthopyronone as a novel analogue of furocoumarin

CHINESE J. ORG. CHEM.-2000-338: Synthesis and structure characterization of two thienonaphthopyrones (SS)

CHINESE J. ORG. CHEM. 2006-504: Synthesis and properties of N-butyl-4-(aza-15-crown-5）-1,8-naphthalimide as a fluorescent probe

CHEM. RESEARCH IN CHINESE UNⅣ.-2005-480: A novel photocleaver with long wavelength absorption - Highly efficient antitumor agent: 4-（2-diethylamino -ethylamino)-8-oxo-8H-acenaphtho-[ 1,2-b] pyrrole-9-carbonitrile

CHEM. J. CHINESE UNⅣ.-1996-1399: Syntheses，DNA Intercalation Activities and Molecular Modelling on Structures of Tatramethyldifuronaphthalenes

J. PHOTOCHEM. PHOTOBIO. B-2001-35: Tetra-trifluoroethoxyl zinc phthalocyanine: potential photosensitizer for use in the photodynamic therapy of cancer (SS)

J. PHOTOCHEM. PHOTOBIO. B-2006-221: Isoquino[4,5-bc]acridines: Design,synthesis and evaluation of DNA binding,anti-tumor and DNA photo-damaging ability

J. CHEM. SOC.-PERKIN TRANSACTIONS 2-2000-715: Interaction of naphthyl heterocycles with DNA: effects of thiono and thio groups (SS)

MONATSH CHEM.-1999-1109: Synthesis of novel DNA-intercalating naphthopyrone derivatives with improved water solubility and photophysical properties

BULL. CHEM. SOC. JAPAN-1999-1571: Highly efficient photoinduced DNA cleavage by naphthopyrone hydroperoxides

CHEM. LETT.-2005-696: Novel naphthalimide fluorescent sensors selective for certain proteins on basis of non-covalent interactions between enzyme and inhibitor (SS)

SYNTHESIS-STUTTGART-1999-1109: General synthesis of thioxo-1,8-naphthalimides via thioxo-1,8-naphthalic anhydrides (SS)

HETEROATOM CHEM.-1999-141: The improved synthesis,Diels-Alder reactions,and desulfuration of trithio-1,8-naphthalic anhydride (SS)

POLYMER-2002-5731: Synthesis and photophysical properties of 1,8-naphthalimide-labelled PAMAM as PET sensors of protons and of transition metal ions

CHINESE J. ANAL. CHEM. -2004-837: Studies on the room temperature phosphorescence of halogen naphthalic anhydrides

CHINESE CHEM. LETT.-2004-118: Anthracylmethyl benzoazacrown ether as selective fluorescence sensors for Zn2+

HETEROCYCL. COMMUN.-2003-229: A new class of DNA intercalator and photocleaver: Bis-naphthailimides with bromo and nitro substituents

MONATSH. CHEM.-2003-393: New fluorescent conjugates of uridine nucleoside and substituted 1,8-naphthalimide: Synthesis,weak interactions and solvent effects on spectra

INT. J. BIO. MACROMOL.-2006-59: Study on the interaction between 4-（2-diethylanuno- ethylamino)-8-oxo-8H- acenaphtho[1,2-b]pyrrole-9-carbonitrile and DNA by molecular spectra

J. AGRI. FOOD CHEM.-2007-2288: Synthesis,insecticidal activity,and QSAR of novel nitromethylene neonicotinoids with tetrahydropyridine fixed cis configuration and exo-ring ether modification

J. AGRI. FOOD CHEM.-2006-125: Synthesis and herbicidal activity of novel 3-aminocarbonyl-2-oxazolidinethione derivatives containing a substituted pyridine ring

J. AGRI. FOOD CHEM.-2006-8793: Novel,unnatural benzo-1,2,3-thiadiazole-7-carboxylate elicitors of taxoid biosynthesis (SS,FF)

J. AGRI. FOOD CHEM.-2005-3120: Syntheses,antifeedant activity,and QSAR analysis of new oxa(thia)diazolyl 3（2H)-pyridazinones (SS)

J. AGRI. FOOD CHEM.-2005-3120: Syntheses,Antifeedant Activity,and QSAR Analysis of New Oxa(thia)diazolyl 3（2 H)-Pyridazinones (SS)

J. AGRI. FOOD CHEM.-2003-152: Synthesis and Antifeedant Activity of New Oxadiazolyl 3（2H)-Pyridazinones

J. AGRI. FOOD CHEM.-2001-124: Synthesis and Quantitative Structure-Activity Relationships of New 2,5-Disubstituted-1,3,4-oxadiazoles (FF)

J. AGRI. FOOD CHEM.-2001-5279: Synthesis and Quantitative Structure-Activity Relationships of Fluorine-Containing 4,4-Dihydroxylmethyl-2-aryl imino- oxazo (thiazo)lidines as Trehalase Inhibitors (SS,FF)

J. AGRI. FOOD CHEM.-1999-4415: Quantitative studies on structure-activity relationship of sulfonylurea and benzoylphenylurea type pesticides and their substituents' bioisosterism using synthons' activity contribution (SS,FF)

J. AGRI. FOOD CHEM.-1996-1538: Molecular modeling study on the structure-activity relationship of substituted dibenzoyl-1-tert-butylhydrazines and their structural similarity to 20-hydroxyecdysone

ACS SYMPOSIUM SERIES-2005（892）-273: Oxadiazole derivatives as novel insect-growth regulators: Synthesis and structure-bioactivity relationship (FF)

J. FLUORINE CHEM.-2006-182: Synthesis and herbicidal activities of fluorine-containing 3-pyridylmethyl-2- phenyliminothiazolidine derivatives (SS,FF)

J. FLUORINE CHEM.-2005-297: Synthesis and fungicidal activity of fluorine-containing phenylimino-thiazolidines derivatives (SS,FF)

J. FLUORINE CHEM.-2005-53: Synthesis and biological activities of hydroxyl-protected fluorine-containing 4,4-dihydroxylmethyl-2-aryl-iminothiazolidines (SS,FF)

J. FLUORINE CHEM.-2004-1159: Synthesis and fungicidal activity of Fluorine-containing Phenylimino-thiazolidines Derivatives (SS,FF)

J. FLUORINE CHEM.-2004-1609: Syntheses,structures and bioactivities of fluorine-containing phenylimino-thia(oxa)zolidine derivatives as agricultural bioregulators (SS,FF)

J. FLUORINE CHEM.-2003-163: Synthesis and insecticidal activities of novel 2,5-disubstituted 1,3,4-oxadiazoles (FF)

J. FLUORINE CHEM.-2003-51: Synthesis and insecticidal activity of new substituted N-aryl-N’-benzoylthiourea compounds (SS,FF)

J. FLUORINE CHEM.-2002-63: Syntheses and insecticidal activity of new 2-（5-(trifluoromethyl)pyridyloxymethyl) -1,3,4-oxadiazoles] (FF)

J. FLUORINE CHEM.-2000-111: Fluorine containing heterocyclic compounds: synthesis of 6-substituted-2-substituted-aryl-1,2,4-triazolo[5,1-b] 1,3,5- thia- diazin-7-one derivatives (SS,FF)

J. FLUORINE CHEM.-2000-173: Syntheses and insecticidal activities of novel 2-fluorophenyl-5-aryl/cyclopropyl-1,3,4-oxadiazoles (FF)

J. FLUORINE CHEM.-2001-143: Synthesis and biological activities of fluorine-containing N,N’-diphenylcarbamimidothioates (SS,FF)

J. FLUORINE CHEM.-1999-39: Syntheses and characterization of 2-amino-5-aryl-1,3,4-oxadiazoles containing trifluoroethoxy groups (FF)

J. FLUORINE CHEM.-1998-9: Polyfluoroalkoxylation and methoxylation of polychloropyridines (FF)

J. FLUORINE CHEM.-1996-9: Alcoholysis of trifluoromethyl groups attached to the pyridine ring (FF)

J. FLUORINE CHEM.-1991-143: A synthetic and MO-SCF study of the trifluoroethoxylation of chloro(trifluoromethyl)pyridine derivatives (FF)

CHEM. PHYS. LETT.-2003-489: Intramolecular noncovalent force in cyclic amidines: nonbonded interaction between carbon atoms and heteroatoms (SS,FF)

PEST. MANAG. SCI. -2003-933: The toxic and anti-feedant activity of 2H-pyridazin-3-one-substituted 1,3,4-oxadiazoles against the armyworm Pseudaletia separata (Walker) and other insects and mite

CARBOHYDRATE RESEARCH-2001-79: Syntheses and activities as trehalase inhibitors of N-arylglycosylamines derived from fluorinated anilines (FF)

J. CHEM. TECH. BIOTECH.-1996-124: Syntheses and insecticidal activities of novel 2,5-disubstituted-1,3,4-oxadiazoles (FF)

CAN. J. CHEM. -2003-272: N'-tert-Butyl-N'-aroyl-N-(alkoxycarbonylmethyl)-N-aroylhydrazines,a novel nonsteroidal ecdysone agonist: syntheses,insecticidal activity,conformational and crystal structure analysis

MONATSH CHEM.-2006-779: An efficient and practical method for the synthesis of 1-（2,6-difluorobenzoyl)-3-（2-alkyl-3-oxopyridazin-4-yl)ureas as potential chitin synthesis inhibitors (FF)

MONATSH CHEM.-2000-953: Novel fused heterocycles: Synthesis and activity of 5,6-dihydro-7-thia-1,3,3a,5-tetraazainden-4-one and 1-thia-3,4a,9-triazafluoren-4-one derivatives (SS)

J. CHEM. RES.-2006- 626: Synthesis and bioactivities of novel neonicotinoids dioxolane compounds

J. CHEM. RES.-2000-88: The crystal structure of 1-phenyl-3-methyl-5-[2 '-（4 ''-phenylmethoxylphenyl)ethoxyl]pyrazole,a potential insect juvenile hormone mimic

J. CHEM. RES.-1999-66: The crystal structure of N-（5-phenyl-1,3,4-oxadiazol-2-yl)-N '-benzoyl urea,a novel insect-growth regulator

J. CHEM. RES. -1998-478: Crystal structure of 1-（3,5-dichloro-2,4-difluorophenyl)-3-（2,6-difluorobenzoyl)urea,an inhibitor of chitin synthesis

CHEM. J. CHINESE UNⅣ.-1994-224: Synthesis and bioactivities of novel trifluoromethylpyridine derivatives

CHINESE CHEM. LETT. -2004-7: Novel Analogues of -Terthienyl，Thienyl 1，3，4-Thia(oxa)diazoles as Potential Photoactivated Insecticides：Synthesis and Bioactivity (SS)

PESTICIDE BIOCHEM. PHYSIOLOGY-2004-42: Photolarvicidal effect of thienyl 1,3,4-thia(oxa)diazoles and their potential DNA photocleavage (SS)

ARKⅣOC-2003-141: Synthesis and insecticidal activity of 1,2,4-triazole derivatives

CHEM. LETT.-2001-54: A Novel and Practical Amination of 4,5-Dichloropyridazin-3-ones via Reduction with Hydrazine Hydrate

ORG. PREP. PROCEDURE INTL.-2000-571: A facile synthesis of aryl isothiocyanates from arylamines (SS)

ORG. PREP. PROCEDURE INTL.-1999-110: A facile synthesis of 3-chloro-4-（2 ',2 ',2 '-trifluoroethoxy)benzonitrile (FF)

CHEM. COMMUN.-2006-865: Baker's yeast-mediated enantioselective reduction of substituted fluorenones

CHEM. COMMUN.-2005-2338: A novel strategy for the preparation of arylhydroxylamines: chemoselective reduction of aromatic nitro compounds using bakers' yeast

CHEM. COMMUN.-2004-2339: A novel strategy for the preparation of arylhydroxylamines: chemoselective reduction of aromatic nitro compounds using bakers’ yeast

APPL. MICROBIO. BIOT.-2005-98: A novel synthetic fluoro-containing jasmonate derivative acts as a chemical inducing signal for plant secondary metabolism (FF)

APPL. MICROBIOL. BIOT.-2006-164: Novel synthetic 2,6-dichloroisonicotinate derivatives as effective elicitors for inducing the biosynthesis of plant secondary metabolites

APPLIED MICROBIO.BIOTECH.-2006-298: Efficient induction of ginsenoside biosynthesis and alteration of ginsenoside heterogeneity in cell cultures of Panax notoginseng by using chemically synthesized 2-hydroxyethyl jasmonate

BIOORG. MED. CHEM. LETT.-2005-1769: Novel 2-aminothiazonaphthalimides as visible light activatable photonucleases: effects of intercalation,heterocyclic-fused area and side chains (SS)

BIOORG. MED. CHEM. LETT.-2003-3513: Thiadiazole: A new family of intercalative photonuclease with electron transfer and radical mechanisms (SS,FF)

BIOORG. MED. CHEM. LETT.-2004-2665: Highly-efficient DNA photocleavers with long wavelength absorptions: thio-heterocyclic fused naphthalimides containing aminoalkyl side chains (SS)

BIOORG. MED. CHEM. LETT.-2004-2335: N-aroyloxylthioxo-naphthalimides as DNA photocleavers of aroyloxyl oxygen radicals: synthesis,evaluation,and substituents' effect (SS)

BIOORG. MED. CHEM. LETT.-2004-4755: Novel fluoro- and hydroxyl-containing jasmonate derivatives as highly efficient elicitors in suspension cultures of Taxus chinensis (FF)

BIOORG. MED. CHEM. LETT.-2006-803: Hydrolysis of plasmid DNA and RNA by amino alkyl naphthalimide as metal-free artificial nuclease (SS)

BIOORG. MED. CHEM.-2006-2935: Novel fluorescent markers for hypoxic cells of naphthalimides with two heterocyclic side chains for bioreductive binding

BIOORG. MED. CHEM.-2006-23: Eliminating nucleic acids contaminants by hydrogen peroxide-induced free radicals during the preparation of proteins (SS)

BIOTECH. BIOENG-2005-516: Highly efficient strategy for enhancing taxoid production by repeated elicitation with a newly synthesized jasmonate in fed- batch cultivation of Taxus chinensis cells

BIOTECH. BIOENG.-2004-809: Novel chemically synthesized hydroxyl-containing jasmonates as powerful inducing signals for plant secondary metabolism

BIOTECH. BIOENG.-2004-595: Novel synthetic jasmonates as highly efficient elicitors for taxoid production by suspension cultures of Taxus chinensis

BIOTECH. PROGR.-2006-331: Novel chemically synthesized salicylate derivative as an effective elicitor for inducing the biosynthesis of plant secondary metabolites

BIOTECH. AND BIOPROCESS ENGI.-2005-162: Efficient elicitation of ginsenoside biosynthesis in cell cultures of Panax notoginseng by using self-chemically-synthesized jasmonates

BIOCHEM. ENGINEERING. J.-2006-23: Eliminating nucleic acids contaminants by hydrogen peroxide-induced free radicals during the preparation of proteins

TETRAHEDRON LETT.-2004-1247: Naphthalimide-thiazoles as novel photonucleases: molecular design,synthesis,and evaluation (SS)

TETRAHEDRON-2005-11264: Versatile acenaphtho[1,2-b]pyrrol-carbonitriles as a new family of heterocycles: diverse Snar(H)H reactions,cytotoxicity and spectral behavior (SS)

DYES AND PIGMENTS-1999-139: Naphthalimide hydroperoxides as photonucleases: substituent effects and structural basis

以上参考资料来源^[4]

钱旭红著有《未来无限》人物传记。^[2]

2002年1月至2010年1月钱旭红兼任上海市化学生物学重点实验室主任，2003年3月至2006年兼任国家南方农药创制中心(上海) 主任。2007年担任中国化工学会副理事长。^[4]2007年至2008年，钱旭红担任亚洲及太平洋化工联盟主席。^[1]2020年11月，基础教育教学指导委员会成立，钱旭红为委员之一。^[7]如今，钱旭红担任中国化学会农业化学专业委员会主任。^[8]

2021年4月16日，钱旭红在清华大学参加健康工程系列论坛第六讲“改变思维”讲座，110余位师生在线上线下参加活动。^[9]

2023年6月14日，华东师范大学举行党委理论学习中心组学习（扩大）会议，钱旭红作题为《超限：引领育人创新的理念与探索》的专题辅导报告，重点围绕时代命题、改变思维、超越学科、超限跃迁四个部分内容，系统分析了拔尖创新人才培养面临的困境。^[10]

钱旭红金句迭出，思维敏捷；言辞幽默，犀利又高远。读他的随笔，听他指点学术思维的江山，听各类质疑的声音，会感觉到这是一位生活在多维时空中的创新者，所到之处，便是张力。这位研究仿生农药的院士，自小形成的叛逆、不服输和好挑战如影相随。用候机飞行中点滴时间，他享受着用笔思考的心灵自由和幸福，在参悟科学精神的质疑、人文精神的关爱的同时，自我加持地推行着信仰精神。（《文汇报》评）^[2]

钱旭红父母都是师范学校毕业的，当年父亲写剧本，他看剧本。家里有许多“小人书”，他一本接着一本看，爱不释手。外公房间偷藏的《红楼梦》，他也会去偷看。从小对文科的热爱为他打下了扎实的文学基础，也令他始终保有着阅读的习惯和兴趣。^[11]

高考前三个月，因父母不同意他考文科，于是只好改考理工科。1978年，钱旭红进入了华东化工学院的化工专业。^[12]

钱旭红酷爱看动画片，逛商场的时候，看到有商家在播动画片，他会被吸引，停下脚步去观赏，以至于猛然发现自己已经混迹于孩童中间而不自知。“动画片把人的想像力无限放大，突破了凡世的种种禁锢gù束缚，而且看的时候心情愉快，可以提升人的幸福感。”他给予了动画片很高的评价。“皇帝的新衣只有小孩才能看得到。做学问必须要纯真，才能看到真实的模样。”^[11]

2021年7月27日，钱旭红在第二十三届中国科协年会中国科技峰会上做主旨演讲，强调了首席技术官（CTO）的重要性，为探索培养可推广可复制的中国特色高技术转化产业化领袖英才提出了建议。^[13]

2021年10月16日，钱旭红作为校长在华东师范大学70周年校庆大会上发表讲话。^[14]