Crystallography Open Database

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1556372 CIFC48 H44 Cu2 O12P -110.53; 10.579; 10.773
109.248; 93.156; 106.287
1073Sunil, Abraham C.; Langner, Ernst H. G.; Marais, Charlene; Bezuidenhoudt, Barend C. B.
Thermo-analytical determination of intermediates in the copper catalysed rearrangement of o-toluic acid to meta-cresol
Catalysis Science & Technology, 2013, 3, 2227
1556373 CIFC19 H24 Br2 Cl2 N4 NiC 2 2 2114.2034; 11.5066; 14.6836
90; 90; 90
2399.8Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556374 CIFC18 H22 Cl2 N4 NiP -19.2765; 10.7428; 12.1287
110.976; 96.346; 113.712
986.47Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556375 CIFC18 H22 Br2 N4 NiP -19.3446; 14.994; 15.681
75.599; 78.411; 81.522
2073.7Budhai, Asheena; Omondi, Bernard; Ojwach, Stephen O.; Obuah, Collins; Osei-Twum, Emmanuel Y.; Darkwa, James
Tandem ethylene oligomerisation and Friedel‒Crafts alkylation of toluene catalysed by bis-(3,5-dimethylpyrazol-1-ylmethyl)benzene nickel(ii) complexes and ethylaluminium dichloride
Catalysis Science & Technology, 2013, 3, 3130
1556376 CIFC45 H41 Br2 Cl N2 NiP 1 21/c 19.6013; 16.927; 24.799
90; 100.77; 90
3959.4Jia, Dedong; Zhang, Wenjuan; Liu, Weiliang; Wang, Lin; Redshaw, Carl; Sun, Wen-Hua
Unsymmetrical α-diiminonickel bromide complexes: synthesis, characterization and their catalytic behavior toward ethylene
Catalysis Science & Technology, 2013, 3, 2737
1556377 CIFC47 H45 Br2 Cl N2 NiP 1 21/c 19.922; 16.84; 24.975
90; 98.41; 90
4128.1Jia, Dedong; Zhang, Wenjuan; Liu, Weiliang; Wang, Lin; Redshaw, Carl; Sun, Wen-Hua
Unsymmetrical α-diiminonickel bromide complexes: synthesis, characterization and their catalytic behavior toward ethylene
Catalysis Science & Technology, 2013, 3, 2737
1556378 CIFC25 H35 N3 ZnP -19.6343; 9.6463; 14.2834
76.36; 88.829; 63.062
1144.29Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556379 CIFC31 H39 N3 O ZnP 1 21/n 112.765; 16.025; 13.594
90; 98.6; 90
2750Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556380 CIFC35 H47 N3 O ZnP -110.889; 14.2911; 20.7227
92.804; 92.129; 92.212
3216.1Dai, Zhongran; Zhang, Jinjin; Gao, Yuan; Tang, Ning; Huang, Yong; Wu, Jincai
Synthesis and structures of tridentate β-diketiminato zinc phenoxides as catalysts for immortal ring-opening polymerization of l-lactide
Catalysis Science & Technology, 2013, 3, 3268
1556381 CIFC3 H5 Au Cl4 N2P 1 2/m 13.8864; 7.7824; 7.5103
90; 98.573; 90
224.61de Almeida, M. Peixoto; Martins, L. M. D. R. S.; Carabineiro, S. A. C.; Lauterbach, T.; Rominger, F.; Hashmi, A. S. K.; Pombeiro, A. J. L.; Figueiredo, J. L.
Homogeneous and heterogenised new gold C-scorpionate complexes as catalysts for cyclohexane oxidation
Catalysis Science & Technology, 2013, 3, 3056
1556382 CIFC14 H16 N2 O2P 1 21/n 15.8113; 23.7797; 9.2207
90; 95.959; 90
1267.33Ray, Suman; Bhaumik, Asim; Dutta, Arghya; Mukhopadhyay, Chhanda
Porous silica nanoparticles with mesoscopic void spaces for the domino intermolecular aerobic oxidative synthesis of novel β,β′-diketoenamines
Catalysis Science & Technology, 2013, 3, 1267
1556383 CIFC99 H102 N9 O6 P Zn3P -3 c 120.8644; 20.8644; 52.9489
90; 90; 120
19961.8Jacobs, Ivo; van Duin, Adri C. T.; Kleij, Arjan W.; Kuil, Mark; Tooke, Duncan M.; Spek, Anthony L.; Reek, Joost N. H.
Conformational studies of ligand-template assemblies and the consequences for encapsulation of rhodium complexes and hydroformylation catalysis
Catalysis Science & Technology, 2013, 3, 1955
1556384 CIFC25.63 H25.25 Cl3.25 Fe N6 O8P 1 21/c 112.2117; 20.6062; 23.4209
90; 90.957; 90
5892.7Wong, Emma; Jeck, Jonathan; Grau, Michaela; White, Andrew J. P.; Britovsek, George J. P.
A strong-field pentadentate ligand in iron-based alkane oxidation catalysis and implications for iron(iv) oxo intermediates
Catalysis Science & Technology, 2013, 3, 1116
1556385 CIFC48 H47 Cl4 Fe2 N11 O18P 1 21/c 112.4043; 38.877; 12.3737
90; 117.208; 90
5306.9Wong, Emma; Jeck, Jonathan; Grau, Michaela; White, Andrew J. P.; Britovsek, George J. P.
A strong-field pentadentate ligand in iron-based alkane oxidation catalysis and implications for iron(iv) oxo intermediates
Catalysis Science & Technology, 2013, 3, 1116
1556599 CIFC87.5 H82 Ag2 Fe O7.5 P4P 1 21 113.2313; 30.795; 18.556
90; 94.183; 90
7540.6Liu, Kuan-Guan; Rouhani, Farzaneh; Gao, Xue-Mei; Abbasi-Azad, Mahsa; Li, Jing-Zhe; Hu, Xiu-De; Wang, Wei; Hu, Mao-Lin; Morsali, Ali
Bilateral photocatalytic mechanism of dye degradation by a designed ferrocene-functionalized cluster under natural sunlight
Catalysis Science & Technology, 2020, 10, 757-767
1556600 CIFC122.5 H108.5 Cu2 Fe O7 P6P b c a24.582; 20.281; 40.461
90; 90; 90
20172Liu, Kuan-Guan; Rouhani, Farzaneh; Gao, Xue-Mei; Abbasi-Azad, Mahsa; Li, Jing-Zhe; Hu, Xiu-De; Wang, Wei; Hu, Mao-Lin; Morsali, Ali
Bilateral photocatalytic mechanism of dye degradation by a designed ferrocene-functionalized cluster under natural sunlight
Catalysis Science & Technology, 2020, 10, 757-767
1556927 CIFC9 H19 I2 N3 PdC 1 2/c 114.7908; 7.8079; 27.592
90; 99.197; 90
3145.5Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556928 CIFC13 H21 I2 N3 PdP 1 21/c 117.5721; 12.5994; 8.4655
90; 99.55; 90
1848.27Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556929 CIFC15 H17 I2 N3 PdC 1 2/c 121.6545; 8.657; 20.1671
90; 95.408; 90
3763.8Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1556930 CIFC16 H19 I2 N3 PdP -19.5333; 10.964; 11.3716
62.48; 79.571; 67.896
976.59Khazipov, Oleg V.; Shevchenko, Maxim A.; Pasyukov, Dmitry V.; Chernenko, Andrey Yu.; Astakhov, Alexander V.; Tafeenko, Victor A.; Chernyshev, Victor M.; Ananikov, Valentine P.
Preventing Pd‒NHC bond cleavage and switching from nano-scale to molecular catalytic systems: amines and temperature as catalyst activators
Catalysis Science & Technology, 2020, 10, 1228-1247
1557055 CIFC20 H21 B Cl2 O2C 1 2/c 127.001; 6.0841; 25.1455
90; 108.298; 90
3922Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557056 CIFC22 H27 B O2C 1 2/c 135.07; 6.2286; 20.596
90; 119.212; 90
3926.8Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557057 CIFC22 H27 B O2P c a 2125.447; 6.3811; 24.281
90; 90; 90
3942.7Rami, Fabian; Bächtle, Franziska; Plietker, Bernd
Hydroboration of internal alkynes catalyzed by FeH(CO)(NO)(PPh3)2: a case of boron-source controlled regioselectivity
Catalysis Science & Technology, 2020, 10, 1492-1497
1557058 CIFC36.5 H57 B Cl F4 N4 P4 RhP 31 2 113.824; 13.824; 40.089
90; 90; 120
6635Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557059 CIFC27 H42 B Cl2 F4 N2 P2 RhP 1 21 19.7105; 14.3281; 11.2851
90; 96.031; 90
1561.44Cunillera, Anton; de los Bernardos, Miriam Díaz; Urrutigoïty, Martine; Claver, Carmen; Ruiz, Aurora; Godard, Cyril
Efficient synthesis of chiral γ-aminobutyric esters via direct rhodium-catalysed enantioselective hydroaminomethylation of acrylates
Catalysis Science & Technology, 2020, 10, 630-634
1557155 CIFC116 H154 Cl N9 O9 Ti2P 1 21/n 126.5998; 13.18144; 32.7719
90; 104.629; 90
11118.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557156 CIFC30 H44 Cl2 O2 TiP 1 21 111.0509; 9.6943; 14.8668
90; 108.131; 90
1513.61Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557157 CIFC220 H283 Cl6 N15 O20 Ti6P -117.651; 18.2749; 19.8507
67.4531; 68.6833; 73.3966
5428.93Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557158 CIFC125 H172.5 Cl N8.5 O9 Ti2P -117.4371; 17.7765; 21.1345
100.63; 93.526; 104.426
6195.8Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557159 CIFC120 H164 Cl2 N6 O8 Ti2P -112.5697; 18.1183; 27.5282
104.559; 98.781; 102.093
5792.04Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557160 CIFC108 H140 Cl N7 O9 Ti2P -113.9465; 17.4744; 23.5392
85.6028; 74.2347; 74.5316
5320.83Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557161 CIFC130.71 H174.42 Cl N2.85 O11.43 Ti2P -116.3253; 17.3213; 23.5069
102.481; 91.495; 101.593
6340.9Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557162 CIFC113 H149.5 Cl N7.5 O9 Ti2P 1 21/n 126.6007; 13.18235; 32.7812
90; 104.622; 90
11122.7Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557163 CIFC49 H61 Cl N2 O4 TiP -112.14575; 18.0271; 21.0909
95.2564; 105.355; 90.2869
4432.27Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557164 CIFC54 H72 Cl2 N2 O4 TiC 1 2/c 143.9803; 12.41683; 19.4608
90; 94.9954; 90
10587.1Sun, Ziyue; Zhao, Yanxia; Santoro, Orlando; Elsegood, Mark R. J.; Bedwell, Elizabeth V.; Zahra, Khadisha; Walton, Alex; Redshaw, Carl
Use of titanocalix[4]arenes in the ring opening polymerization of cyclic esters
Catalysis Science & Technology, 2020, 10, 1619-1639
1557173 CIFC54.28 H49.13 Ir O0.28 P3P 1 21/c 117.31801; 12.99024; 19.71788
90; 94.4442; 90
4422.5Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557174 CIFC57 H68 Cl2 Ir2 N4 O S2P 1 21/c 112.9317; 16.6; 25.5365
90; 90.2757; 90
5481.76Tickner, Ben J.; Semenova, Olga; Iali, Wissam; Rayner, Peter J.; Whitwood, Adrian C.; Duckett, Simon B.
Optimisation of pyruvate hyperpolarisation using SABRE by tuning the active magnetisation transfer catalyst.
Catalysis science & technology, 2020, 10, 1343-1355
1557528 CIFC39 H72 Cd Mo12 N6 O68 P8 Zn2P -113.126; 25.198; 30.034
113.698; 101.194; 90.634
8879Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557529 CIFC26 H24 Cd1.2 Co0.8 Mo12 N4 Na4 O69 P8C 1 2/c 121.0842; 18.3743; 21.9022
90; 100.716; 90
8337.1Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557530 CIFC65 H116 Al2 Cd2 Mo24 N10 O137 P16P 1 n 115.882; 21.676; 25.338
90; 94.559; 90
8695.2Tian, Xuerui; Zhang, Yaqi; Ma, Yuanyuan; Zhao, Qing; Han, Zhangang
Hourglass-type polyoxometalate-based crystalline materials as efficient cooperating photocatalysts for the reduction of Cr(vi) and oxidation of dyes
Catalysis Science & Technology, 2020, 10, 2593-2601
1557594 CIFC16 H22 Cl2 Co N4 O4P 1 21/n 19.5079; 32.3832; 13.8528
90; 110.045; 90
4006.9Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557595 CIFC17 H22 Cl2 Co N4 O4P 1 21/c 112.2832; 7.3066; 22.5865
90; 95.779; 90
2016.8Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557596 CIFC41 H44 B Cl Co N4P 21 21 219.8205; 14.0434; 26.706
90; 90; 90
3683.1Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557597 CIFC43 H46 B Cl Co N4P 1 21/c 116.0327; 10.7162; 22.6792
90; 107.025; 90
3725.7Anandababu, Karunanithi; Muthuramalingam, Sethuraman; Velusamy, Marappan; Mayilmurugan, Ramasamy
Single-step benzene hydroxylation by cobalt(ii) catalysts via a cobalt(iii)-hydroperoxo intermediate
Catalysis Science & Technology, 2020, 10, 2540-2548
1557658 CIFC36 H46 Cl10 Fe4 N6 O9P 1 21/n 113.612; 13.537; 14.409
90; 109.931; 90
2496.1Karim, Suhana; Chakraborty, Aratrika; Samanta, Debabrata; Zangrando, Ennio; Ghosh, Totan; Das, Debasis
A dinuclear iron complex as an efficient electrocatalyst for homogeneous water oxidation reaction
Catalysis Science & Technology, 2020, 10, 2830-2837
1557659 CIFC32 H40 Cl4 Fe2 N6 O10P 1 21/c 111.8719; 16.9617; 9.4064
90; 102.136; 90
1851.81Karim, Suhana; Chakraborty, Aratrika; Samanta, Debabrata; Zangrando, Ennio; Ghosh, Totan; Das, Debasis
A dinuclear iron complex as an efficient electrocatalyst for homogeneous water oxidation reaction
Catalysis Science & Technology, 2020, 10, 2830-2837
1557722 CIFC36 H46 N4 O6 P2P -19.437; 10.4908; 18.5143
96.9776; 99.2858; 104.161
1728.97Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557723 CIFC27 H30 Br2 Co N4 O7 S2P -18.1545; 11.7917; 16.3115
107.981; 96.136; 103.72
1421.47Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557724 CIFC26 H28 Br2 Co N4 O4P 1 21/n 18.0833; 11.8214; 13.6272
90; 95.751; 90
1295.61Weder, Nicola; Probst, Benjamin; Sévery, Laurent; Fernández-Terán, Ricardo J.; Beckord, Jan; Blacque, Olivier; Tilley, S. David; Hamm, Peter; Osterwalder, Jürg; Alberto, Roger
Mechanistic insights into photocatalysis and over two days of stable H2 generation in electrocatalysis by a molecular cobalt catalyst immobilized on TiO2
Catalysis Science & Technology, 2020, 10, 2549-2560
1557862 CIFC20 H35 Al N6P n a 2118.8949; 10.1078; 23.9918
90; 90; 90
4582.1Navarro, Marta; Sánchez-Barba, Luis F.; Garcés, Andrés; Fernández-Baeza, Juan; Fernández, Israel; Lara-Sánchez, Agustín; Rodríguez, Ana M.
Bimetallic scorpionate-based helical organoaluminum complexes for efficient carbon dioxide fixation into a variety of cyclic carbonates
Catalysis Science & Technology, 2020, 10, 3265-3278
1557863 CIFC33.5 H44 Al2 N6P 1 21/c 118.637; 9.384; 26.354
90; 125.325; 90
3760.4Navarro, Marta; Sánchez-Barba, Luis F.; Garcés, Andrés; Fernández-Baeza, Juan; Fernández, Israel; Lara-Sánchez, Agustín; Rodríguez, Ana M.
Bimetallic scorpionate-based helical organoaluminum complexes for efficient carbon dioxide fixation into a variety of cyclic carbonates
Catalysis Science & Technology, 2020, 10, 3265-3278
1557983 CIFC23 H33 Br Ir N3 OP 1 21/c 18.5663; 11.0966; 24.1272
90; 98.595; 90
2267.7González-Lainez, Miguel; Jiménez, M. Victoria; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.
Effective N-methylation of nitroarenes with methanol catalyzed by a functionalized NHC-based iridium catalyst: a green approach to N-methyl amines
Catalysis Science & Technology, 2020, 10, 3458-3467
1557984 CIFC17 H21 Br Ir N3 O3P -19.2294; 11.1211; 11.892
99.157; 110.946; 114.394
968.3González-Lainez, Miguel; Jiménez, M. Victoria; Passarelli, Vincenzo; Pérez-Torrente, Jesús J.
Effective N-methylation of nitroarenes with methanol catalyzed by a functionalized NHC-based iridium catalyst: a green approach to N-methyl amines
Catalysis Science & Technology, 2020, 10, 3458-3467
1558022 CIFC15 H19 N O6 SP b c a13.3705; 7.2739; 31.8622
90; 90; 90
3098.78Wu, Xiao-Yun; Gui, Hou-Ze; Jangra, Harish; Wei, Yin; Zipse, Hendrik; Shi, Min
Phosphine-catalyzed [3 + 2] annulation of 2-aminoacrylates with allenoates and mechanistic studies
Catalysis Science & Technology, 2020, 10, 3959-3964
1558045 CIFC23 H22 F9 Fe N10 O9 S3P -19.1084; 11.7267; 16.3308
85.341; 89.88; 70.285
1636.05Dyckhoff, Florian; Schlagintweit, Jonas F.; Reich, Robert M.; Kühn, Fritz E.
Pushing the limits of activity and stability: the effects of Lewis acids on non-heme iron‒NHC epoxidation catalysts
Catalysis Science & Technology, 2020, 10, 3532-3536
1558072 CIFC15 H19 N2 O4 ReP 1 21/c 114.6069; 8.871; 12.0927
90; 90.801; 90
1566.79Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558073 CIFC23 H35 N2 O4 ReC 1 2/c 123.927; 9.4928; 22.1646
90; 106.575; 90
4825.1Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558074 CIFC15 H18 N3 O6 ReP b c a8.90063; 11.9803; 31.8099
90; 90; 90
3391.96Li, Jing; Lutz, Martin; Klein Gebbink, Robertus J. M.
N,N,O-Coordinated tricarbonylrhenium precatalysts for the aerobic deoxydehydration of diols and polyols
Catalysis Science & Technology, 2020, 10, 3782-3788
1558149 CIFC28 H24 Co N2 O10 S2C 1 2/c 120.1441; 12.2778; 11.4937
90; 92.993; 90
2838.8Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558150 CIFC28 H24 Co0.79 Fe0.21 N2 O10 S2C 1 2/c 120.1868; 12.2668; 11.4817
90; 92.862; 90
2839.64Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558151 CIFC28 H24 Co0.29 N2 Ni0.71 O10 S2C 1 2/c 120.1616; 12.1398; 11.4274
90; 92.792; 90
2793.63Yang, Chun; Cai, Wen-Jing; Yu, Bin-Bin; Qiu, Hong; Li, Meng-Li; Zhu, Lian-Wen; Yan, Zheng; Hou, Lei; Wang, Yao-Yu
Performance enhancement of oxygen evolution reaction through incorporating bimetallic electrocatalysts in two-dimensional metal‒organic frameworks
Catalysis Science & Technology, 2020, 10, 3897-3903
1558164 CIFC16 H29 Cl F6 N2 O P Ru SbP 1 21/n 111.7394; 14.7656; 14.6955
90; 108.172; 90
2420.26González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558165 CIFC17 H31 Cl F6 N2 O P Ru SbP 1 21/n 18.3717; 21.574; 14.8558
90; 105.025; 90
2591.39González-Fernández, Rebeca; Álvarez, Daniel; Crochet, Pascale; Cadierno, Victorio; Menéndez, M. Isabel; López, Ramón
Catalytic hydration of cyanamides with phosphinous acid-based ruthenium(ii) and osmium(ii) complexes: scope and mechanistic insights
Catalysis Science & Technology, 2020, 10, 4084-4098
1558270 CIFC70.98 H100.97 Fe2 N4 O7.98 Ti2P 1 21/c 122.6283; 8.7736; 18.5643
90; 105.17; 90
3557.2Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558271 CIFC39 H57.63 Fe N2 O4 ZrP 1 21/c 122.8642; 9.1582; 19.4463
90; 106.447; 90
3905.3Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558272 CIFC31.51 H58.93 N2 O4 ZrP -19.0808; 9.9464; 21.5037
93.147; 91.175; 115.995
1741Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558273 CIFC30.5 H58 N2 O4 TiP 1 21/c 126.1034; 13.6068; 18.7389
90; 90.427; 90
6655.6Doerr, Alicia M.; Burroughs, Justin M.; Legaux, Nicholas M.; Long, Brian K.
Redox-switchable ring-opening polymerization by tridentate ONN-type titanium and zirconium catalysts
Catalysis Science & Technology, 2020, 10, 6501-6510
1558490 CIFC95 H104 B2 Cl2 Co2 F10 O12 P6P b c a26.2086; 27.5599; 28.9629
90; 90; 90
20920.1Papa, Veronica; Cabrero-Antonino, Jose R.; Spannenberg, Anke; Junge, Kathrin; Beller, Matthias
Homogeneous cobalt-catalyzed deoxygenative hydrogenation of amides to amines
Catalysis Science & Technology, 2020, 10, 6116-6128
1558540 CIFC19 H21 Cl2 N RuP c a 217.1672; 13.7037; 17.9697
90; 90; 90
1764.93Chatterjee, Basujit; Kalsi, Deepti; Kaithal, Akash; Bordet, Alexis; Leitner, Walter; Gunanathan, Chidambaram
One-pot dual catalysis for the hydrogenation of heteroarenes and arenes
Catalysis Science & Technology, 2020, 10, 5163-5170
1558696 CIFC30 H47 Cl Ir NP 1 21/c 110.1037; 11.6662; 23.623
90; 97.789; 90
2758.8Zhang, Dejin; Yang, Guoqiang; Zhao, Yue; Shao, Shouyan; Zhu, Guisheng; Liu, Peijun; Liu, Jia; Hu, Xingbang; Zhang, Zhibing
Efficient methanol carbonylation to methyl acetate catalyzed by a cyclic(alkyl)(amino)carbene iridium complex
Catalysis Science & Technology, 2020, 10, 6045-6049
1558697 CIFC24 H35 Cl I0 Ir N O2P 1 21/n 19.4294; 15.2306; 16.4958
90; 94.904; 90
2360.38Zhang, Dejin; Yang, Guoqiang; Zhao, Yue; Shao, Shouyan; Zhu, Guisheng; Liu, Peijun; Liu, Jia; Hu, Xingbang; Zhang, Zhibing
Efficient methanol carbonylation to methyl acetate catalyzed by a cyclic(alkyl)(amino)carbene iridium complex
Catalysis Science & Technology, 2020, 10, 6045-6049
1559097 CIFC25 H19 NP 1 21/n 18.7417; 11.0177; 19.073
90; 101.123; 90
1802.48Nori, Valeria; Dasgupta, Ayan; Babaahmadi, Rasool; Carlone, Armando; Ariafard, Alireza; Melen, Rebecca L.
Triarylborane catalysed N-alkylation of amines with aryl esters
Catalysis Science & Technology, 2020, 10, 7523-7530
1559098 CIFC23 H19 F2 NP 1 21/c 18.9007; 11.1893; 18.1967
90; 93.764; 90
1808.35Nori, Valeria; Dasgupta, Ayan; Babaahmadi, Rasool; Carlone, Armando; Ariafard, Alireza; Melen, Rebecca L.
Triarylborane catalysed N-alkylation of amines with aryl esters
Catalysis Science & Technology, 2020, 10, 7523-7530
1559113 CIFC65 H89 In N2 O3 P2P 1 21/c 115.1464; 16.9612; 26.1549
90; 103.943; 90
6521.25Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559114 CIFC50 H74 N2 O2 P2P -111.4385; 15.3688; 15.4343
83.413; 78.85; 78.526
2600.66Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559115 CIFC57 H85 In N2 O5 P2P 21 21 2111.128; 18.2363; 30.9376
90; 90; 90
6278.28Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559116 CIFC65 H87 In N2 O4 P2P n a 2120.6809; 18.5748; 15.7154
90; 90; 90
6036.97Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559117 CIFC63 H102 In N2 O3 P2P 1 21/n 110.9894; 28.7519; 19.81
90; 91.214; 90
6257.9Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559118 CIFC52 H77 In N2 O3 P2P -114.2993; 14.3196; 17.8201
105.16; 107.065; 96.826
3290.3Yuntawattana, Nattawut; McGuire, Thomas M.; Durr, Christopher B.; Buchard, Antoine; Williams, Charlotte K.
Indium phosphasalen catalysts showing high isoselectivity and activity in racemic lactide and lactone ring opening polymerizations
Catalysis Science & Technology, 2020, 10, 7226-7239
1559240 CIFC18 H32 Co O4 PP -19.1926; 18.6959; 18.8899
93.315; 103.878; 98.222
3105Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559241 CIFC15 H8 Co F18 O4 PP -18.808; 11.2727; 11.4608
87.2767; 86.0751; 81.5105
1122.03Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559242 CIFC27 H40 Co O6 PP 1 21/c 19.342; 12.6826; 22.4709
90; 93.041; 90
2658.6Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559243 CIFC24 H40 Co O6 PP 1 21/n 110.925; 12.6105; 20.1341
90; 104.561; 90
2684.77Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559244 CIFC21 H34 Co N2 O6 PP 1 21/c 117.748; 8.4442; 16.239
90; 91.117; 90
2433.2Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559245 CIFC33 H29 Co N O5 PP 21 21 2110.7864; 11.5313; 22.3359
90; 90; 90
2778.2Fischer, Fabian; Pientka, Tobias; Jiao, Haijun; Spannenberg, Anke; Hapke, Marko
CpCo(i) precatalysts for [2 + 2 + 2] cycloaddition reactions: synthesis and reactivity
Catalysis Science & Technology, 2020, 10, 8005-8014
1559279 CIFC58 H53 Cl3 Cu F6 N2 O5 P3C 1 2/c 135.7359; 12.1275; 27.9938
90; 112.354; 90
11220.4Li, Chenfei; Dickson, Robert; Rockstroh, Nils; Rabeah, Jabor; Cordes, David B.; Slawin, Alexandra M. Z.; Hünemörder, Paul; Spannenberg, Anke; Bühl, Michael; Mejía, Esteban; Zysman-Colman, Eli; Kamer, Paul C. J.
Ligand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry reaction
Catalysis Science & Technology, 2020, 10, 7745-7756
1559280 CIFC57 H40 Cu F18 N2 O P3P 1 21/n 111.4434; 20.2661; 27.9804
90; 99.805; 90
6394.24Li, Chenfei; Dickson, Robert; Rockstroh, Nils; Rabeah, Jabor; Cordes, David B.; Slawin, Alexandra M. Z.; Hünemörder, Paul; Spannenberg, Anke; Bühl, Michael; Mejía, Esteban; Zysman-Colman, Eli; Kamer, Paul C. J.
Ligand electronic fine-tuning and its repercussion on the photocatalytic activity and mechanistic pathways of the copper-photocatalysed aza-Henry reaction
Catalysis Science & Technology, 2020, 10, 7745-7756
1559301 CIFC21.5 H32 Cl2 N3 O2.5 RuP 1 21/n 112.5519; 23.6646; 16.9746
90; 94.02; 90
5029.7Das, Kanu; Yasmin, Eileen; Das, Babulal; Srivastava, Hemant Kumar; Kumar, Akshai
Phosphine-free pincer-ruthenium catalyzed biofuel production: high rates, yields and turnovers of solventless alcohol alkylation
Catalysis Science & Technology, 2020, 10, 8347-8358
1559302 CIFC14 H21 Cl2 N3 O2 RuP 1 21/c 19.2304; 10.8098; 18.2395
90; 96.278; 90
1809Das, Kanu; Yasmin, Eileen; Das, Babulal; Srivastava, Hemant Kumar; Kumar, Akshai
Phosphine-free pincer-ruthenium catalyzed biofuel production: high rates, yields and turnovers of solventless alcohol alkylation
Catalysis Science & Technology, 2020, 10, 8347-8358
1559556 CIFC68 H156 O28 Si14 Zr2P -113.346; 17.309; 23.753
86.026; 89.28; 76.624
5325.4Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559557 CIFC96 H184 O28 Si14 Zr2P b c a20.0054; 24.0516; 27.5739
90; 90; 90
13267.5Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559558 CIFC68 H156 Hf2 O28 Si14P b c a18.563; 22.017; 26.445
90; 90; 90
10808Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559559 CIFC96 H184 Hf2 O28 Si14P b c a20.061; 24.064; 27.568
90; 90; 90
13308Garg, Shipra; Unruh, Daniel K.; Krempner, Clemens
Zirconium and hafnium polyhedral oligosilsesquioxane complexes ‒ green homogeneous catalysts in the formation of bio-derived ethers via a MPV/etherification reaction cascade
Catalysis Science & Technology, 2021, 11, 211-218
1559560 CIFC86 H109 N9 Na2 O11 V2P -113.4214; 14.2596; 25.2549
85.709; 78.946; 69.251
4435.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559561 CIFC104 H120 N8 O8 V2P -112.0966; 12.3373; 17.8971
90.8728; 107.997; 99.2458
2501.28Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559562 CIFC80 H90 Cl2 N2 O8 V2P 1 21/n 119.7039; 20.0862; 20.6921
90; 113.114; 90
7532Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559563 CIFC178 H213 N11 O20 V4P -114.0354; 17.3396; 20.1906
71.168; 84.459; 66.456
4260.59Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559564 CIFC86 H114 N6 O16 V4P -112.4983; 13.6976; 14.1554
68.166; 79.128; 75.546
2165.92Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559565 CIFC82 H90 F6 N2 O8 V2P 1 21/c 120.0005; 19.9315; 22.023
90; 116.08; 90
7885.4Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636
1559566 CIFC355 H421 Cl2 N21 O32 V8P -119.7899; 20.6775; 22.7696
69.271; 76.567; 78.627
8407.9Xing, Tian; Prior, Timothy J.; Elsegood, Mark R. J.; Semikolenova, Nina V.; Soshnikov, Igor E.; Bryliakov, Konstantin; Chen, Kai; Redshaw, Carl
Vanadium complexes derived from oxacalix[6]arenes: structural studies and use in the ring opening homo-/co-polymerization of ε-caprolactone/δ-valerolactone and ethylene polymerization
Catalysis Science & Technology, 2021, 11, 624-636

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