We demonstrate the control of electron-electron correlation in frustrated double ionization (FDI) of the two-electron triatomic molecule D + 3 when driven by two orthogonally polarized two-color laser fields. We employ a three-dimensional semi-classical model that fully accounts for the electron and nuclear motion in strong fields. We analyze the FDI probability and the distribution of the momentum of the escaping electron along the polarization direction of the longer wavelength and more intense laser field. These observables when considered in conjunction bear clear signatures of the prevalence or absence of electron-electron correlation in FDI, depending on the time-delay between the two laser pulses. We find that D + 3 is a better candidate compared to H 2 for demonstrating also experimentally that electron-electron correlation indeed underlies FDI.PACS numbers: 33.80. Rv, 34.80.Gs, 42.50.Hz Frustrated double ionization (FDI) is a major process in the nonlinear response of multi-center molecules when driven by intense laser fields, accounting roughly for 10% of all ionization events [1,2]. In frustrated ionization an electron first tunnel-ionizes in the driving laser field. Then, due to the electric field of the laser pulse, it is recaptured by the parent ion in a Rydberg state [3]. This process is a candidate for the inversion of N 2 in free-space air lasing [4]. In FDI an electron escapes and another one occupies a Rydberg state at the end of the laser pulse. In theoretical studies of strongly-driven two-electron diatomic and triatomic molecules, two pathways of FDI have been identified [2,8]. Electron-electron correlation is important, primarily, for one of the two pathways. It is well accepted that electron-electron correlation underlies a significant part of double ionization in strongly-driven molecules-a mechanism known as non-sequential double ionization [9,10]. However, electron-electron correlation in FDI has yet to be accessed experimentally.Here, we propose a road for future experiments to identify the important role of electron-electron correlation in FDI. We identify the parameters of orthogonally polarized two-color (OTC) laser fields that best control the relevant pathway for electron-electron correlation in FDI. We demonstrate traces of attosecond control of electron motion in space and time in two observables of FDI as a function of the time-delay between the fundamental 800 nm and the second harmonic 400 nm laser field. We show that, together, the FDI probability and the momentum of the escaping electron along the fundamental laser field bear clear signatures of the turning on and off of electronelectron correlation.Two-color laser fields are an efficient tool for controlling electron motion [11,12] and for steering the outcome of chemical reactions [13][14][15]. Other applications include the field-free orientation of molecules [16][17][18], the generation of high-harmonic spectra [19][20][21][22] and probing atomic and molecular orbital symmetry [23][24][25]. The strongly-driven dynam...