Crystallography Open Database

Result: there are 369 entries in the selection

Switch to the old layout of the page

Download all results as: list of COD numbers | list of CIF URLs | data in CSV format | archive of CIF files (ZIP)

Searching journal of publication like 'RSC Advances' volume of publication is 15

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 4 | Next 100 Right arrow | Last Right arrow Right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

COD ID Blue up arrow Links Formula Up arrow Space group Up arrow Cell parameters Cell volume Up arrow Bibliography
7251132 CIFC8 H21 B I N3 OP 1 21/c 19.6367; 12.7626; 11.3363
90; 107.192; 90
1331.95Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251133 CIFC8 H23 B I N3 OP 1 21/c 110.2265; 9.5381; 14.3703
90; 95.782; 90
1394.57Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251134 CIFC12 H31 B I N3 OP 1 21/c 110.2903; 8.023; 21.9128
90; 102.169; 90
1768.45Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251135 CIFC6 H19 B I N3 OP 1 21/c 19.8683; 15.6874; 7.9504
90; 101.165; 90
1207.49Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251136 CIFC8 H23 B I N3 OP 1 21/n 19.8196; 12.5339; 11.74
90; 96.402; 90
1435.92Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251137 CIFC8 H23 B I N3 OP 1 21/n 111.3609; 7.2321; 17.9361
90; 107.119; 90
1408.4Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251138 CIFC6 H19 B I N3 OP n a 219.9877; 17.8852; 7.0593
90; 90; 90
1261.02Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251139 CIFC5 H17 B F6 N3 O PP n m a11.7816; 8.5561; 13.0621
90; 90; 90
1316.72Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251140 CIFC7 H21 B I N3 OP 1 21/n 16.8276; 18.2829; 10.3532
90; 93.525; 90
1289.93Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251141 CIFC9 H21 B F6 N4 O5 S2P 1 21/c 18.9317; 22.3717; 9.821
90; 90.539; 90
1962.32Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251142 CIFC33 H43 B2 N3 OP b c a19.249; 16.089; 19.492
90; 90; 90
6037Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251143 CIFC8 H19 B F6 N4 O5 S2P 1 21/n 18.544; 9.321; 47.36
90; 90.952; 90
3771Crowley, Margaret E.; Merchant, Gabriel A.; Davis, James H.; Stachurski, Christopher D.; Zeller, Matthias; Salter, E. A.; Wierzbicki, A.; Trulove, Paul C.; Durkin, David P.; Kingrey, Grace L.; Escalante, Edgar E.; O'Brien, Richard A.; Whillock, Novita M.
Ureas are identified as the first neutral O-donors broadly effective in stabilizing ionic liquids and other salts of boron-centred cations: synthesis and detailed characterization
RSC Advances, 2025, 15, 40519-40527
7251144 CIFC20 H17 O4P 1 21/c 110.731; 5.879; 24.449
90; 94.21; 90
1538.3Falasca, Valerio; Yee, Eugene; Sabir, Shekh; Bhadbade, Mohan; Wenholz, Daniel S.; StC Black, David; Kumar, Naresh
Synthesis and biological evaluation of pyrano and furano fused ring isoflavene derivatives.
RSC advances, 2025, 15, 40149-40163
7251145 CIFC15 H21 N O6P 1 21 15.1486; 11.036; 14.01
90; 94.408; 90
793.7Halder, Tapas; Hore, Ratul; Das, Susanta; Sett, Subhadip; Maity, Joykrishna
Acid-catalysed rearrangement of acyl groups: synthesis of β-d-gluco aminocyclopentitols and carbanucleoside derivatives.
RSC advances, 2025, 15, 40390-40399
7251146 CIFC20 H22.33 N O5.67P 1 21 117.9551; 7.5298; 20.8678
90; 98.955; 90
2786.9Halder, Tapas; Hore, Ratul; Das, Susanta; Sett, Subhadip; Maity, Joykrishna
Acid-catalysed rearrangement of acyl groups: synthesis of β-d-gluco aminocyclopentitols and carbanucleoside derivatives.
RSC advances, 2025, 15, 40390-40399
7251147 CIFC33 H26 Cl6 F N O3C 1 2/c 123.3655; 9.5263; 30.8642
90; 108.24; 90
6524.8Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251148 CIFC40.5 H34.5 Au Cl F N2 O2P -114.66; 15.507; 15.652
89.298; 89.61; 88.852
3557.2Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251149 CIFC31 H22 Au Cl F N O2P 1 21/c 112.9318; 13.3667; 15.7531
90; 110.458; 90
2551.3Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251150 CIFC35.5 H34 Au Cl2 F N2 O2P 43 21 29.543; 9.543; 70.4724
90; 90; 90
6417.8Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251151 CIFC32 H24 Au Cl3 F N O2P 1 21/n 17.0291; 31.375; 40.124
90; 91.392; 90
8846.3Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251152 CIFC35 H33 Au Cl F N2 O2P 1 21/c 114.262; 17.54; 12.714
90; 107.296; 90
3036.7Dietl, Martin C.; Hüßler, Christopher; Scherr, Matthias; Frederiksen, Zoé M.; Graf, Jürgen; Rominger, Frank; Rudolph, Matthias; Caligiuri, Isabella; Tripodi, Laura; Rizzolio, Flavio; Scattolin, Thomas; Hashmi, A. Stephen K.
Synthesis of azulenyl-substituted gold(i)-carbene complexes and investigation of their anticancer activity
RSC Advances, 2025, 15, 41260-41269
7251153 CIFC30 H25 N O4P -110.9981; 11.306; 11.7371
107.674; 102.727; 113.268
1177Devaraj, Thangaraj; Srinivasan, Kannupal
Three-component reaction of formyl-substituted donor-acceptor cyclopropanes, primary aromatic amines and 2-naphthol: access to cyclopropane fused 2-pyrrolidinone derivatives.
RSC advances, 2025, 15, 39689-39695
7251154 CIFC12 H8 Cl4 Co N4P 41 21 26.8311; 6.8311; 36.092
90; 90; 90
1684.19Khachroum, Hajer; Rhaiem, Abdallah Ben; Abdelbaky, Mohammed S. M.; García-Granda, Santiago; Dammak, Mohamed
Next-generation cobalt hybrid material: structural, luminescence, and dielectric properties for advanced functional applications.
RSC advances, 2025, 15, 40687-40697
7251155 CIFC10 H26 Br8 N2 SnP b c a12.792; 12.973; 14.605
90; 90; 90
2423.7Elghoul, Amal; Ben Salah, Bochra; Hajlaoui, Fadhel; Karoui, Karim; Audebrand, Nathalie; Roisnel, Thierry; Kozma, Erika; Botta, Chiara; Zouari, Nabil
Investigation on the structural, optical, photoluminescence and electric properties of a semiconductor material [Br(CH<sub>2</sub>)<sub>2</sub>N(CH<sub>3</sub>)<sub>3</sub>]<sub>2</sub>SnBr<sub>6</sub>.
RSC advances, 2025, 15, 40199-40208
7251228 CIFC54 H58 Br2 Cu2 N10 O15P -114.0326; 15.3151; 15.7791
102.979; 109.334; 107.627
2843.7Kumari, Pratima; Kumar, Aman; Kataria, Ramesh; Kaushik, Navin Kumar; Ahmed, Mukhtar; Ansari, Azaj; Ekta,; Brahma, Mettle; Maruthi, Mulaka; Babu, Yangala Sudheer; Singh, Bijender; Kumar, Vinod
Synthesis, characterization and biological studies of pyrazole-linked Schiff bases and their copper(ii) complexes as potential therapeutics
RSC Advances, 2025, 15, 42299-42314
7251229 CIFC19 H26 Cl F6 N2 P Ru SP 21 21 219.907; 13.111; 18.3887
90; 90; 90
2388.52Bhunya, Debasis; Datta, Riya; Maity, Ribhu; Saha, Alipe; Sen, Sujata; Brandao, Paula; Pattanayak, Satyajit; Maity, Tithi; Sarkar, Keka; Samanta, Bidhan Chandra
Design and synthesis of bioactive Ru(ii) complexes: antibacterial activity, biocompatibility and biomolecular binding
RSC Advances, 2025, 15, 42573-42587
7251243 CIFC25 H43 Cl P2 SeP 1 21/n 16.6637; 19.2509; 22.2228
90; 95.852; 90
2835.9Aghion, Iulia-Andreea; Septelean, Raluca A.; Lucaci, David; Moraru, Ionut-Tudor; Soran, Albert P.; Ciocan, Catalin C.; Licarete, Emilia; Banciu, Manuela; Nemes, Gabriela
Synthesis and coordination ability of the first phosphavinyl(selenoxo)phosphorane: an electronic story
RSC Advances, 2025, 15, 43426-43435
7251244 CIFC26 H45 Cl5 P2 Pd SeP n m a9.6344; 13.6183; 25.1598
90; 90; 90
3301.1Aghion, Iulia-Andreea; Septelean, Raluca A.; Lucaci, David; Moraru, Ionut-Tudor; Soran, Albert P.; Ciocan, Catalin C.; Licarete, Emilia; Banciu, Manuela; Nemes, Gabriela
Synthesis and coordination ability of the first phosphavinyl(selenoxo)phosphorane: an electronic story
RSC Advances, 2025, 15, 43426-43435
7251245 CIFC21 H21 N3 O5P 31 2 19.5132; 9.5132; 39.0933
90; 90; 120
3063.98Zhang, Guangshuai; Chen, Xin; Liu, Yan; Peng, Rui; Xu, Mengwei; Yan, Si; Xiao, Jin; Liu, Zishu; Min, Qing; Liao, Gang; Wang, Xiaoji; Qin, Shuanglin
NaHMDS/B(C6F5)3-promoted diastereoselective Friedel–Crafts alkylation of indoles/pyrroles with N-tert-butanesulfinylimines: towards the asymmetric synthesis of bisindole alkaloid Calcicamide B
RSC Advances, 2025, 15, 43421-43425
7251246 CIFC17 H18 Bi2 I8 N4 OP -17.5699; 9.652; 11.5436
76.552; 86.66; 84.383
815.82Hrizi, Chakib; Hamdouni, Monia; Essid, Marwa; Nouiri, Mourad; Khatyr, Abderrahim; Knorr, Michael; Viau, Lydie; Schmidt, Annika; Strohmann, Carsten; Chaabouni, Slaheddine
Extending lead-free organic–inorganic semiconducting materials to new polymeric structures: 2,2′-bipyridinium iodoantimonate and quinoxalinium iodobismuthate
RSC Advances, 2025, 15, 43523-43541
7251247 CIFC10 H9 I4 N2 SbC 1 c 112.2685; 18.2626; 7.5924
90; 91.864; 90
1700.21Hrizi, Chakib; Hamdouni, Monia; Essid, Marwa; Nouiri, Mourad; Khatyr, Abderrahim; Knorr, Michael; Viau, Lydie; Schmidt, Annika; Strohmann, Carsten; Chaabouni, Slaheddine
Extending lead-free organic–inorganic semiconducting materials to new polymeric structures: 2,2′-bipyridinium iodoantimonate and quinoxalinium iodobismuthate
RSC Advances, 2025, 15, 43523-43541
7251310 CIFC8 H14 Cl5 N2 SbP 1 21/n 110.8365; 11.8067; 12.0281
90; 106.92; 90
1472.3Alibi, Amin; Elleuch, Nour; Oueslati, Abderrazek; Shova, Sergiu; Boujelbene, Mohamed
Synthesis, optical features, and electrical properties of a new antimony-based hybrid halide (C8H14N2)[SbCl5]
RSC Advances, 2025, 15, 45840-45854
7251311 CIFC13 H15 Cu N3 O6P 1 21/n 18.5673; 10.4935; 16.3022
90; 97.043; 90
1454.52Khan, Md. Adnan; Shruti, Sonal; Sengupta, Swaraj; Khan, Sahanwaj; Bhardwaj, Prabhakar; Kumar, Pankaj; Naskar, Subhendu
Water-soluble binuclear aquo Cu(ii) complex with an amide ligand as an electrocatalyst for the OER, HER and CO2RR
RSC Advances, 2025, 15, 46425-46433
7251312 CIFC13 H15 N3 O5P -18.3624; 8.5232; 9.6931
92.749; 92.29; 96.721
684.61Khan, Md. Adnan; Shruti, Sonal; Sengupta, Swaraj; Khan, Sahanwaj; Bhardwaj, Prabhakar; Kumar, Pankaj; Naskar, Subhendu
Water-soluble binuclear aquo Cu(ii) complex with an amide ligand as an electrocatalyst for the OER, HER and CO2RR
RSC Advances, 2025, 15, 46425-46433
7251313 CIFC17 H13 N O3P 1 21/n 110.0247; 10.2858; 13.4724
90; 110.611; 90
1300.25Miwa, Marino; Ito, Akitaka
Fluorescent solvatochromism and nonfluorescence processes of charge-transfer-type molecules with a 4-nitrophenyl moiety
RSC Advances, 2025, 15, 46297-46307
7251314 CIFC17 H14 OP 1 21/c 111.5001; 17.6022; 5.9565
90; 94.087; 90
1202.69Miwa, Marino; Ito, Akitaka
Fluorescent solvatochromism and nonfluorescence processes of charge-transfer-type molecules with a 4-nitrophenyl moiety
RSC Advances, 2025, 15, 46297-46307
7251315 CIFC52 H99 N30 O36I 428.306; 28.306; 18.617
90; 90; 90
14916Rincón, David A; Zaorska, Ewelina; Malinska, Maura
Halogenated <i>N</i>-phenylpiperazine and 2-(piperazin-1-yl)pyrimidine as novel cucurbit[7]uril guests: experimental and computational insights into supramolecular binding.
RSC advances, 2025, 15, 45555-45572
7251316 CIFC52 H87 Cl2 F2 N30 O30I 428.6126; 28.6126; 18.3038
90; 90; 90
14985Rincón, David A; Zaorska, Ewelina; Malinska, Maura
Halogenated <i>N</i>-phenylpiperazine and 2-(piperazin-1-yl)pyrimidine as novel cucurbit[7]uril guests: experimental and computational insights into supramolecular binding.
RSC advances, 2025, 15, 45555-45572
7251317 CIFC50 H71 N32 Na3.5 O35P n n 228.9179; 26.6083; 10.629
90; 90; 90
8178.5Rincón, David A; Zaorska, Ewelina; Malinska, Maura
Halogenated <i>N</i>-phenylpiperazine and 2-(piperazin-1-yl)pyrimidine as novel cucurbit[7]uril guests: experimental and computational insights into supramolecular binding.
RSC advances, 2025, 15, 45555-45572
7251318 CIFC73 H182 Cl F N44 O74C 2 2 2132.4607; 39.283; 20.2199
90; 90; 90
25783.5Rincón, David A; Zaorska, Ewelina; Malinska, Maura
Halogenated <i>N</i>-phenylpiperazine and 2-(piperazin-1-yl)pyrimidine as novel cucurbit[7]uril guests: experimental and computational insights into supramolecular binding.
RSC advances, 2025, 15, 45555-45572
7251340 CIFC12 H10 N2 O2 SP n a 2119.4454; 5.3607; 10.9087
90; 90; 90
1137.13Pavić, Luka; Miočić, Filip; Razum, Marta; Sarjanović, Josipa; Pisk, Jana
From structure to function: tunable electrical and catalytic properties in rare Mo(vi)-thiophene-2-carboxylic acid hydrazone complexes obtained mechanochemically
RSC Advances, 2025, 15, 46194-46206
7251341 CIFC15 H16 Mo N2 O6 SP 1 21/c 17.7429; 10.6417; 21.2775
90; 91.132; 90
1752.87Pavić, Luka; Miočić, Filip; Razum, Marta; Sarjanović, Josipa; Pisk, Jana
From structure to function: tunable electrical and catalytic properties in rare Mo(vi)-thiophene-2-carboxylic acid hydrazone complexes obtained mechanochemically
RSC Advances, 2025, 15, 46194-46206
7251342 CIFC13 H12 Mo N2 O5 SP b c n14.8458; 7.2875; 26.5865
90; 90; 90
2876.36Pavić, Luka; Miočić, Filip; Razum, Marta; Sarjanović, Josipa; Pisk, Jana
From structure to function: tunable electrical and catalytic properties in rare Mo(vi)-thiophene-2-carboxylic acid hydrazone complexes obtained mechanochemically
RSC Advances, 2025, 15, 46194-46206
7251360 CIFC26 H22 F6 N2 O2P -19.5617; 10.833; 11.9272
96.483; 106.465; 99.458
1151.9Akhtar, Nasim; Lekanne Deprez, Siebe; Jayawardana, Senuri G.; Davis, Macallister; Fonseca Guerra, Célia; García-López, Víctor
From amides to thioamides: understanding enhanced anion binding in acyclic receptors
RSC Advances, 2025, 15, 46908-46913
7251361 CIFC30 H28 Cl0 N2 O2P 1 21/n 19.5813; 27.725; 9.8074
90; 114.246; 90
2375.4Akhtar, Nasim; Lekanne Deprez, Siebe; Jayawardana, Senuri G.; Davis, Macallister; Fonseca Guerra, Célia; García-López, Víctor
From amides to thioamides: understanding enhanced anion binding in acyclic receptors
RSC Advances, 2025, 15, 46908-46913
7251362 CIFC12 H9 Cl F N O3P -17.1404; 8.9074; 9.3379
72.15; 81.114; 85.545
558.25Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251363 CIFC14 H13 Cl F N O3P -19.0561; 9.0599; 9.325
69.818; 69.854; 71.629
657.2Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251364 CIFC14 H19 Cl F N O6P -17.8889; 9.0771; 12.3827
99.027; 97.434; 107.192
821.95Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251365 CIFC11 H7 Cl F N O3P -17.1789; 8.4907; 9.3255
73.107; 71.053; 76.278
507.98Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251366 CIFC13 H11 Cl F N O3P 1 21/c 111.992; 25.5932; 8.1786
90; 91.831; 90
2508.8Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251367 CIFC14 H15 Cl F N O4P 1 21/c 14.3523; 15.2232; 22.9957
90; 92.056; 90
1522.6Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251368 CIFC15 H15 Cl F N O3P 1 21/n 110.4187; 11.4345; 12.6311
90; 101.018; 90
1477Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251369 CIFC13 H11 Cl F N O3P -18.2284; 8.97; 9.4084
69.237; 74.254; 69.76
600.4Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251370 CIFC10 H5 Cl F N O3P 1 21/n 16.291; 8.2326; 17.968
90; 97.441; 90
922.7Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251371 CIFC15 H11 Cl F N4 O3P 1 21/n 18.8502; 20.148; 9.0629
90; 108.764; 90
1530.2Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251372 CIFC15 H14 Cl4 F N O3P 1 21/n 17.2079; 27.556; 9.2363
90; 92.329; 90
1833Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251373 CIFC16 H17 Cl F N O3P 1 21/c 110.2295; 16.2593; 9.9934
90; 113.612; 90
1523Kumar, Satyanand; Kumar, Ravi; Mishra, Rakesh K.; Awasthi, Satish Kumar
Exploring weak noncovalent interactions in a few halo-substituted quinolones.
RSC advances, 2025, 15, 37216-37225
7251374 CIFC39 H28 N2 SeP 1 21/c 110.967; 26.809; 9.828
90; 96.41; 90
2871.5Issac, Jerome; Priyadharsan, R. Rameshbabu; Chidambaranathan, Kamalanathan; Karthikeyan, Subramanian; Moon, Dohyun; Anthony, Savarimuthu Philip; Madhu, Vedichi
Phenyl selenoxide functionalized TPA/TPE π-conjugated imidazo[1,2-<i>a</i>]pyridine: a fluorescent probe for the selective detection of water in organic solvents.
RSC advances, 2025, 15, 44205-44212
7251375 CIFC28 H26 N2 O4C 1 2/c 132.7304; 4.4327; 32.3534
90; 96.961; 90
4659.4Tanbakouchian, Zahra; Zolfigol, Mohammad Ali; Tonekaboni, Maryam-Sadat; Kozakiewicz-Piekarz, Anna; Bikas, Rahman
Regioselective Cu(i)-catalyzed intramolecular hydroacylation and dimerization of propargylarylaldehydes.
RSC advances, 2025, 15, 44254-44259
7251376 CIFC11 H14 N2 O2 SP 1 21 15.8421; 9.9787; 10.4247
90; 101.544; 90
595.43Shandu, Malibongwe P.; Ngwenya, Andile R.; Lamola, Jairus L.; Moshapo, Paseka T.
Base-mediated three-component system for the synthesis of <i>S</i>-substituted <i>N</i>-acyl ureas.
RSC advances, 2025, 15, 44246-44251
7251377 CIFC6 H8 As N O3P 1 21 17.24314; 6.13919; 8.70641
90; 101.075; 90
379.938Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251378 CIFC6 H8 As N O3P 1 21 17.24488; 6.14439; 8.7053
90; 101.106; 90
380.262Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251379 CIFC6 H8 As N O3P 1 21 17.23374; 6.13187; 8.69579
90; 101.094; 90
378.505Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251380 CIFC6 H8 As N O3P 1 21 17.243; 6.13597; 8.70648
90; 101.07; 90
379.741Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251381 CIFC6 H8 As N O3P 1 21 17.24395; 6.13599; 8.70666
90; 101.071; 90
379.799Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251382 CIFC6 H8 As N O3P 1 21 17.23467; 6.13615; 8.69951
90; 101.04; 90
379.051Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251383 CIFC6 H8 As N O3P 1 21 17.24136; 6.13653; 8.70452
90; 101.074; 90
379.599Balmohammadi, Yaser; Metry, Eduardo; Malaspina, Lorraine A.; Cametti, Georgia; Nakamura, Yuiga; Grabowsky, Simon
Interplay between geometry, electron density, and polarizability of the controversial drug atoxyl in crystal and biological environments
RSC Advances, 2025, 15, 46749-46760
7251384 CIFC62 H58 Cu F6 N4 O8 PP -114.7809; 14.8375; 15.4905
115.129; 114.546; 92.324
2698.9Cetin, M. Mustafa; Mazumdar, Arindam; Cordes, David B.; Fidan, Vahap Gazi; Yang, Zhen; Mayer, Michael F.
Rotaxane synthesis via a dynamic [2]catenane-ring-opening, axle-cleaving double cross metathesis
RSC Advances, 2025, 15, 47117-47127
7251385 CIFC62 H58 Cu F6 N4 O8 PP 1 21/c 116.7265; 7.8498; 43.035
90; 96.345; 90
5615.9Cetin, M. Mustafa; Mazumdar, Arindam; Cordes, David B.; Fidan, Vahap Gazi; Yang, Zhen; Mayer, Michael F.
Rotaxane synthesis via a dynamic [2]catenane-ring-opening, axle-cleaving double cross metathesis
RSC Advances, 2025, 15, 47117-47127

Blue left arrow Blue left arrow First | Blue left arrow Previous 100 | of 4 | Next 100 Right arrow | Last Right arrow Right arrow | Display 5 20 50 100 200 300 500 1000 entries per page

Back to the search form
Your own data is not in the COD? Deposit it, thanks!